Immunosuppression codes (persisting)
Codelist metadata
-
Coding system
- SNOMED CT
-
Coding system release
- unknown
-
Organisation
- NHSD Primary Care Domain Refsets
-
Codelist ID
- nhsd-primary-care-domain-refsets/imatrisk1_cod
-
Version Tag
- 20201016
-
Version ID
- 574e4aa7
Versions
About
Description
Taken from the IMATRISK1_COD
refset published by NHSD.
References
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
code | term |
---|---|
10294000 | Reactive mastocytosis |
105601003 | Quantitative disorder of neutrophils |
105602005 | Quantitative abnormality of granulocytes |
10564005 | Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
10755671000119100 | Human immunodeficiency virus in mother complicating childbirth |
10759351000119103 | Sickle cell anemia in mother complicating childbirth |
108631000119101 | History of autologous bone marrow transplant |
1090241000000107 | Angioimmunoblastic T-cell lymphoma with dysproteinaemia |
1091861000000100 | Follicular lymphoma, cutaneous follicle centre |
1091891000000106 | B-cell Hodgkin's lymphoma |
1091921000000103 | B-cell non-Hodgkin's lymphoma |
109962001 | Diffuse non-Hodgkin's lymphoma |
109964000 | Diffuse non-Hodgkin's lymphoma, undifferentiated |
109965004 | Diffuse non-Hodgkin's lymphoma, lymphoblastic |
109966003 | Diffuse non-Hodgkin's lymphoma, immunoblastic |
109967007 | Diffuse non-Hodgkin's lymphoma, small cleaved cell |
109968002 | Diffuse non-Hodgkin's lymphoma, small cell |
109969005 | Diffuse non-Hodgkin's lymphoma, large cell |
109970006 | Follicular non-Hodgkin's lymphoma, small cleaved cell |
109971005 | Follicular non-Hodgkin's lymphoma, mixed small cleaved cell and large cell |
109972003 | Follicular non-Hodgkin's lymphoma, large cell |
109975001 | T-zone lymphoma |
109976000 | Lymphoepithelioid lymphoma |
109977009 | Peripheral T-cell lymphoma |
109978004 | T-cell lymphoma |
109979007 | B-cell lymphoma |
109982002 | Alpha heavy chain disease |
109983007 | Monoclonal gammopathy |
109984001 | Gamma heavy chain disease |
109989006 | Multiple myeloma |
109991003 | Acute myelofibrosis |
109992005 | Polycythemia vera |
109993000 | Chronic myeloproliferative disorder (clinical) |
109995007 | Myelodysplastic syndrome |
109996008 | Myelodysplastic syndrome: Refractory anemia, without ringed sideroblasts, without excess blasts |
109998009 | Refractory anemia with ringed sideroblasts |
110000005 | Refractory anemia with excess blasts in transformation |
110004001 | Acute promyelocytic leukemia, FAB M3 |
110005000 | Acute myelomonocytic leukemia, FAB M4 |
110006004 | Prolymphocytic leukemia |
110007008 | Adult T-cell leukemia/lymphoma |
111037009 | Basophilic hyperplasia |
111396008 | Chédiak-Higashi syndrome |
111583006 | Leukocytosis |
111584000 | Reticular dysgenesis |
111585004 | Neutropenia associated with autoimmune disease |
111587007 | Severe combined immunodeficiency due to absent interleukin-2 receptor |
111684008 | Capsular tear without major disruption of parenchyma of spleen AND with open wound in abdominal cavity |
111880001 | Acute human immunodeficiency virus infection |
11603001 | Sickle cell retinopathy |
116133005 | Congenital agammaglobulinemia |
116691000119101 | Marginal zone lymphoma of spleen |
116811000119106 | Non-Hodgkin lymphoma of central nervous system metastatic to lymph node of lower limb |
116821000119104 | Non-Hodgkin lymphoma of central nervous system metastatic to lymph node of upper limb |
116841000119105 | Marginal zone lymphoma of lymph nodes of multiple sites |
116871000119103 | Mantle cell lymphoma of lymph nodes of multiple sites |
117211000119105 | Peripheral T-cell lymphoma of lymph nodes of multiple sites |
118599009 | Hodgkin's disease |
118600007 | Malignant lymphoma |
118601006 | Non-Hodgkin's lymphoma |
118602004 | Hodgkin's granuloma |
118605002 | Hodgkin lymphoma, nodular lymphocyte predominance |
118606001 | Hodgkin's sarcoma |
118607005 | Hodgkin lymphoma, lymphocyte-rich |
118608000 | Hodgkin's disease, nodular sclerosis |
118609008 | Hodgkin's disease, mixed cellularity |
118610003 | Hodgkin's disease, lymphocytic depletion |
118611004 | Sézary's disease |
118613001 | Hairy cell leukemia |
118615008 | Malignant mast cell tumor |
118617000 | Burkitt's lymphoma |
118618005 | Mycosis fungoides |
119249001 | Agammaglobulinemia |
119250001 | Hypogammaglobulinemia |
121131000119109 | Chronic graft versus host disease after transplantation of bone marrow |
12227007 | Capsular tear without major disruption of parenchyma of spleen AND without open wound into abdominal cavity |
12240661000119103 | Long term systemic steroid user |
12301000132103 | Acute lymphoid leukemia relapse |
12311000132101 | Refractory acute lymphoid leukemia |
123313007 | Alpha heavy chain disease, enteric form |
123617004 | Fleckmilz |
123772008 | Homozygous hemoglobinopathy |
123777002 | Autoimmune leukopenia |
123782009 | Dysgammaglobulinemia |
1239371000000103 | Haemoglobin E beta zero thalassaemia |
1239381000000101 | Haemoglobin E beta plus thalassaemia |
124950009 | Deficiency of immunoglobulin |
12631000119106 | Immunoglobulin G deficiency |
127034005 | Pancytopenia |
127040003 | Sickle cell-hemoglobin SS disease |
127041004 | Sickle cell-beta-thalassemia |
127042006 | Sickle cell beta plus thalassemia |
127043001 | Sickle cell-beta^0^-thalassemia |
127044007 | Sickle cell-delta beta^0^-thalassemia |
127045008 | Sickle cell anemia with coexistent alpha-thalassemia |
127047000 | Sickle cell-hemoglobin Lepore disease |
127048005 | Sickle cell-Hemoglobin O Arab disease |
127066000 | Familial polycythemia vera |
127067009 | Stress neutrophilia |
127220001 | Malignant lymphoma of lymph nodes |
127225006 | Chronic myelomonocytic leukemia |
127230005 | Neoplasm of spleen |
127388009 | Hypergammaglobulinemia |
127911000119105 | Light chain nephropathy due to multiple myeloma |
12814002 | B lymphocyte disorder |
128531006 | Islet cell transplant |
128874001 | Cutaneous CD30+ lymphoproliferative disorder |
128875000 | Primary cutaneous CD30 antigen positive large T-cell lymphoma |
129639005 | Hereditary neutrophilia |
129640007 | Benign granulocytopenia in childhood |
129641006 | Chronic benign neutropenia of childhood |
129642004 | Chronic idiopathic immunoneutropenia in adults |
129643009 | Chronic hypoplastic neutropenia |
129644003 | Myeloperoxidase deficiency syndrome |
129645002 | Adult glucose-6-phosphate dehydrogenase deficiency of leukocytes syndrome |
13048006 | Orbital lymphoma |
13160009 | Complication of transplanted intestines |
133751000119102 | Lymphoma of colon |
13720003 | Triclonal gammopathy |
13886001 | Sickle cell nephropathy |
14024008 | Humoral immunologic aplastic anemia |
14333004 | Alloimmune neonatal neutropenia |
14534009 | Splenic vein thrombosis |
15012007 | Granulocyte abnormality due to immune defect |
1518005 | Splenitis |
152621000119105 | History of allotransplantation of bone marrow |
161626009 | History of splenectomy |
161668009 | History of skin recipient |
16196000 | Cytomegaloviral mononucleosis |
16294009 | Splenomegaly |
16318001000119107 | Hypogammaglobulinemia due to multiple myeloma |
164165007 | On examination - moderate splenomegaly |
164166008 | On examination - gross splenomegaly |
164167004 | On examination - painful splenomegaly |
165531008 | Lymphocytosis - absolute |
165816005 | Human immunodeficiency virus positive |
16618004 | Polyclonal gammopathy |
1671000 | Sago spleen |
16944002 | Mononucleosis syndrome |
17182001 | Agranulocytosis |
17363001 | Splenic sarcoidosis |
174691005 | Transplantation of pancreas and duodenum |
174692003 | Whole organ pancreatic transplant |
174693008 | Transplantation of tail of pancreas |
174694002 | Renewal of transplanted pancreatic tissue |
174776001 | Total splenectomy |
174778000 | Total splenectomy and reimplantation of fragments |
17604001 | Bilateral right-sidedness sequence |
183005 | Autoimmune pancytopenia |
186706006 | Human immunodeficiency virus infection constitutional disease |
186707002 | Human immunodeficiency virus infection with neurological disease |
186708007 | Human immunodeficiency virus infection with secondary clinical infectious disease |
186792002 | Plasmodium vivax malaria with rupture of spleen |
187821001 | Angiosarcoma of spleen |
187822008 | Fibrosarcoma of spleen |
18827005 | Complement abnormality |
188487008 | Lymphosarcoma and reticulosarcoma |
188489006 | Reticulosarcoma of lymph nodes of head, face and neck |
188492005 | Reticulosarcoma of lymph nodes of axilla and upper limb |
188493000 | Reticulosarcoma of lymph nodes of inguinal region and lower limb |
188498009 | Lymphosarcoma |
188500005 | Lymphosarcoma of lymph nodes of head, face and neck |
188501009 | Lymphosarcoma of intrathoracic lymph nodes |
188502002 | Lymphosarcoma of intra-abdominal lymph nodes |
188503007 | Lymphosarcoma of lymph nodes of axilla and upper limb |
188504001 | Lymphosarcoma of lymph nodes of inguinal region and lower limb |
188505000 | Lymphosarcoma of intrapelvic lymph nodes |
188506004 | Lymphosarcoma of spleen |
188507008 | Lymphosarcoma of lymph nodes of multiple sites |
188510001 | Burkitt's lymphoma of lymph nodes of head, face and neck |
188511002 | Burkitt's lymphoma of intrathoracic lymph nodes |
188512009 | Burkitt's lymphoma of intra-abdominal lymph nodes |
188513004 | Burkitt's lymphoma of lymph nodes of axilla and upper limb |
188514005 | Burkitt's lymphoma of lymph nodes of inguinal region and lower limb |
188515006 | Burkitt's lymphoma of intrapelvic lymph nodes |
188516007 | Burkitt's lymphoma of spleen |
188517003 | Burkitt's lymphoma of lymph nodes of multiple sites |
188524002 | Hodgkin's paragranuloma of intrathoracic lymph nodes |
188526000 | Hodgkin's paragranuloma of intra-abdominal lymph nodes |
188529007 | Hodgkin's paragranuloma of intrapelvic lymph nodes |
188531003 | Hodgkin's paragranuloma of lymph nodes of multiple sites |
188534006 | Hodgkin's granuloma of lymph nodes of head, face and neck |
188536008 | Hodgkin's granuloma of intra-abdominal lymph nodes |
188537004 | Hodgkin's granuloma of lymph nodes of axilla and upper limb |
188538009 | Hodgkin's granuloma of lymph nodes of inguinal region and lower limb |
188541000 | Hodgkin's granuloma of lymph nodes of multiple sites |
188544008 | Hodgkin's sarcoma of lymph nodes of head, face and neck |
188547001 | Hodgkin's sarcoma of lymph nodes of axilla and upper limb |
188548006 | Hodgkin's sarcoma of lymph nodes of inguinal region and lower limb |
188551004 | Hodgkin's sarcoma of lymph nodes of multiple sites |
188554007 | Hodgkin's disease, lymphocytic-histiocytic predominance of lymph nodes of head, face and neck |
188558005 | Hodgkin's disease, lymphocytic-histiocytic predominance of lymph nodes of axilla and upper limb |
188559002 | Hodgkin's disease, lymphocytic-histiocytic predominance of lymph nodes of inguinal region and lower limb |
188562004 | Hodgkin's disease, lymphocytic-histiocytic predominance of lymph nodes of multiple sites |
188565002 | Hodgkin's disease, nodular sclerosis of lymph nodes of head, face and neck |
188566001 | Hodgkin's disease, nodular sclerosis of intrathoracic lymph nodes |
188567005 | Hodgkin's disease, nodular sclerosis of intra-abdominal lymph nodes |
188568000 | Hodgkin's disease, nodular sclerosis of lymph nodes of axilla and upper limb |
188569008 | Hodgkin's disease, nodular sclerosis of lymph nodes of inguinal region and lower limb |
188570009 | Hodgkin's disease, nodular sclerosis of intrapelvic lymph nodes |
188572001 | Hodgkin's disease, nodular sclerosis of lymph nodes of multiple sites |
188575004 | Hodgkin's disease, mixed cellularity of lymph nodes of head, face and neck |
188576003 | Hodgkin's disease, mixed cellularity of intrathoracic lymph nodes |
188577007 | Hodgkin's disease, mixed cellularity of intra-abdominal lymph nodes |
188578002 | Hodgkin's disease, mixed cellularity of lymph nodes of axilla and upper limb |
188579005 | Hodgkin's disease, mixed cellularity of lymph nodes of inguinal region and lower limb |
188580008 | Hodgkin's disease, mixed cellularity of intrapelvic lymph nodes |
188582000 | Hodgkin's disease, mixed cellularity of lymph nodes of multiple sites |
188585003 | Hodgkin's disease, lymphocytic depletion of lymph nodes of head, face and neck |
188586002 | Hodgkin's disease, lymphocytic depletion of intrathoracic lymph nodes |
188587006 | Hodgkin's disease, lymphocytic depletion of intra-abdominal lymph nodes |
188589009 | Hodgkin's disease, lymphocytic depletion of lymph nodes of axilla and upper limb |
188590000 | Hodgkin's disease, lymphocytic depletion of lymph nodes of inguinal region and lower limb |
188591001 | Hodgkin's disease, lymphocytic depletion of intrapelvic lymph nodes |
188592008 | Hodgkin's disease, lymphocytic depletion of spleen |
188593003 | Hodgkin's disease, lymphocytic depletion of lymph nodes of multiple sites |
188609000 | Nodular lymphoma of lymph nodes of head, face and neck |
188612002 | Nodular lymphoma of lymph nodes of axilla and upper limb |
188613007 | Nodular lymphoma of lymph nodes of inguinal region and lower limb |
188627002 | Mycosis fungoides of lymph nodes of multiple sites |
188630009 | Sézary's disease of lymph nodes of head, face and neck |
188631008 | Sézary's disease of intrathoracic lymph nodes |
188632001 | Sézary's disease of intra-abdominal lymph nodes |
188633006 | Sézary's disease of lymph nodes of axilla and upper limb |
188634000 | Sézary's disease of lymph nodes of inguinal region and lower limb |
188635004 | Sézary's disease of intrapelvic lymph nodes |
188637007 | Sézary's disease of lymph nodes of multiple sites |
188645002 | Leukemic reticuloendotheliosis of lymph nodes of head, face and neck |
188648000 | Leukemic reticuloendotheliosis of lymph nodes of axilla and upper limb |
188649008 | Leukemic reticuloendotheliosis of lymph nodes of inguinal region and lower limb |
188672005 | Follicular non-Hodgkin's mixed small cleaved and large cell lymphoma |
188674006 | Diffuse malignant lymphoma - small non-cleaved cell |
188675007 | Malignant lymphoma - small cleaved cell |
188676008 | Malignant lymphoma - mixed small and large cell |
188679001 | Diffuse non-Hodgkin's lymphoma undifferentiated (diffuse) |
188718006 | Malignant plasma cell neoplasm, extramedullary plasmacytoma |
188725004 | Lymphoid leukemia |
188726003 | Subacute lymphoid leukemia |
188728002 | Aleukemic lymphoid leukemia |
188729005 | Adult T-cell leukemia |
188732008 | Myeloid leukemia |
188733003 | Chronic eosinophilic leukemia |
188734009 | Chronic neutrophilic leukemia |
188736006 | Subacute myeloid leukemia |
188737002 | Chloroma |
188741003 | Aleukemic myeloid leukemia |
188744006 | Monocytic leukemia |
188745007 | Chronic monocytic leukemia |
188746008 | Subacute monocytic leukemia |
188748009 | Aleukemic monocytic leukemia |
188754005 | Megakaryocytic leukemia |
188768003 | Myelomonocytic leukemia |
188770007 | Subacute myelomonocytic leukemia |
190030009 | Compound leukemias |
19058002 | Congestive splenomegaly |
190808009 | Polyclonal hypergammaglobulinemia |
190817009 | Macroglobulinemia |
190818004 | Waldenström macroglobulinemia |
190923000 | Sporadic primary amyloidosis |
190959006 | Hemophagocytic lymphohistiocytosis due to infection |
190979003 | Selective immunoglobulin A deficiency |
190980000 | Selective immunoglobulin M deficiency |
190981001 | Selective immunoglobulin G deficiency |
190986006 | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia |
190993005 | Autosomal recessive severe combined immunodeficiency |
190995003 | Thymic aplasia or dysplasia with immunodeficiency |
190996002 | Severe combined immunodeficiency with reticular dysgenesis |
190997006 | Severe combined immunodeficiency with low T- and B-cell numbers |
190998001 | Severe combined immunodeficiency with low or normal B-cell numbers |
191001007 | Major histocompatibility complex class I deficiency |
191002000 | Major histocompatibility complex class II deficiency |
191011000 | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions |
191012007 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
191013002 | Common variable immunodeficiency with autoantibodies to B- or T-cells |
191018006 | Lymphocyte function antigen-1 defect |
191244003 | Aplastic anemia due to chronic disease |
191246001 | Aplastic anemia due to infection |
191247005 | Aplastic anemia caused by radiation |
191248000 | Aplastic anemia caused by toxic cause |
191256002 | Idiopathic aplastic anemia |
191273000 | Leukemoid reaction of the newborn |
191338000 | Primary splenic neutropenia |
191345000 | Acquired neutropenia in newborn |
191347008 | Cyclical neutropenia |
191357009 | Eosinophilic disorder |
191358004 | Hereditary eosinophilia |
191360002 | Drug-induced eosinophilia |
191382009 | Chronic congestive splenomegaly |
193370005 | Proliferative retinopathy due to sickle cell disease |
19636003 | Monocytosis |
197478000 | Congenital celiac disease |
197479008 | Acquired celiac disease |
19944001 | Autologous bone marrow transplant without purging |
20224008 | Delta heavy chain disease |
203436008 | Osteoporosis in multiple myelomatosis |
203592006 | X-linked severe combined immunodeficiency |
205735005 | Hypoplasia of spleen |
210180009 | Closed injury of spleen |
21043008 | Neutrophil cytomatrix disorder |
213148006 | Transplanted organ rejection |
21527007 | Chronic granulomatous disease, type IV |
22310002 | Chronic idiopathic monocytosis |
22406001 | Severe combined immunodeficiency due to absent lymphoid stem cells |
228311000000103 | Allograft of bone marrow from haploidentical donor |
22996003 | Splenic infarction |
230180003 | Human immunodeficiency virus leukoencephalopathy |
230586003 | Neuropathy due to multiple myeloma |
230598008 | Neuropathy caused by human immunodeficiency virus |
23132008 | Amyloid light-chain amyloidosis |
232033003 | Sickle cell-hemoglobin C retinopathy |
232075002 | Lymphoma of retina |
23238000 | Common variable agammaglobulinemia |
23269001 | Double heterozygous sickling disorder |
233691007 | Asthmatic pulmonary eosinophilia |
233692000 | Cryptogenic pulmonary eosinophilia |
234319005 | Splenectomy |
234331007 | Syngeneic bone marrow transplant |
234332000 | T-cell depleted allogeneic bone marrow graft |
234333005 | Imperfect T-cell depleted allogeneic bone marrow graft |
234334004 | Allogeneic related bone marrow transplant |
234335003 | Allogeneic unrelated bone marrow transplant |
234367000 | Pancytopenia with pancreatitis |
234391009 | Sickle cell anemia with high hemoglobin F |
234416002 | X-linked hypogammaglobulinemia |
234417006 | T-cell lymphocytosis |
234418001 | Chronic benign granulocytopenia |
234423001 | Chronic benign neutropenia |
234424007 | Metabolic neutropenia |
234425008 | Autoimmune neutropenia |
234426009 | Corticosteroid-induced neutrophilia |
234427000 | Monocytoid disorder |
234428005 | Lymphocytoid disorder |
234429002 | Chemotactic disorder |
234430007 | CR3-receptor deficiency |
234431006 | Specific granule deficiency |
234433009 | Myeloperoxidase deficiency |
234434003 | Alders syndrome |
234435002 | Hereditary hypersegmentation |
234436001 | Hemolytic erythrophagocytic syndrome |
234437005 | Hemophagocytic lymphohistiocytosis |
234502009 | Cystic dermoid choristoma of spleen |
234503004 | Hydatid cyst of spleen caused by Echinococcus |
234510005 | Amyloidosis of spleen |
234511009 | Post-splenectomy disorder |
234512002 | Post-splenectomy thrombocytosis |
234513007 | Post-splenectomy leukocytosis |
234519006 | Bone marrow transplant rejection |
234520000 | Bone marrow transplant failure |
234522008 | Disease relapse in transplant marrow |
234532001 | Immunodeficiency disorder |
234533006 | X-linked agammaglobulinemia with growth hormone deficiency |
234534000 | Autosomal agammaglobulinemia with absent B-cells |
234537007 | Autosomal recessive hyperimmunoglobulin M syndrome |
234539005 | Immunoglobulin heavy chain deficiency |
234540007 | Selective immunoglobulin E deficiency |
234541006 | Selective immunoglobulin D deficiency |
234542004 | Selective immunoglobulin M and immunoglobulin A deficiency |
234543009 | Immunoglobulin light chain deficiency |
234544003 | Immunoglobulin subclass deficiency |
234546001 | Immunoglobulin G2 deficiency |
234547005 | Combined immunoglobulin G2 and G4 deficiency |
234548000 | Immunoglobulin G3 deficiency |
234549008 | Immunoglobulin G4 deficiency |
234550008 | Immunoglobulin G1 deficiency |
234551007 | Immunoglobulin A1 deficiency |
234552000 | Immunoglobulin A2 deficiency |
234553005 | Immunoglobulin-associated molecule deficiency |
234554004 | Secretory piece deficiency |
234555003 | Defective immunoglobulin glycosylation |
234556002 | Specific antibody deficiency |
234557006 | Anti-polysaccharide antibody deficiency |
234558001 | Anti-haemophilus influenzae B polysaccharide antibody deficiency |
234559009 | Anti-pneumococcal polysaccharide antibody deficiency |
234560004 | Anti-meningococcal polysaccharide A antibody deficiency |
234561000 | Anti-meningococcal polysaccharide C antibody deficiency |
234562007 | Anti-protein antibody deficiency |
234563002 | Anti-staphylococcal antibody deficiency |
234564008 | Primary immunoglobulin catabolism abnormality |
234565009 | Immunoglobulin hypercatabolism |
234566005 | Familial immunoglobulin hypercatabolism |
234570002 | Severe combined immunodeficiency with maternofetal engraftment |
234571003 | Warts, hypogammaglobulinemia, infections, and myelokathexis |
234572005 | Benign combined immunodeficiency |
234573000 | Phagocytic cell defect |
234574006 | Disorder of phagocytic cell number |
234576008 | Chronic familial neutropenia |
234577004 | Lipochrome histiocytosis - familial |
234578009 | Defective phagocytic cell opsonization |
234579001 | Mannan-binding protein deficiency |
234580003 | Defective phagocytic cell chemotaxis |
234581004 | Defective phagocytic cell adhesion |
234582006 | Leukocyte adhesion deficiency - type 1 |
234583001 | Leukocyte adhesion deficiency - type 2 |
234584007 | Tuftsin deficiency |
234585008 | Defective phagocytic cell killing |
234586009 | Leukocyte glucose-6-phosphate dehydrogenase deficiency |
234587000 | Neutrophil lactoferrin deficiency |
234588005 | Neutrophil secondary granule deficiency |
234589002 | Glutathione synthetase deficiency |
234590006 | Gluthathione peroxidase deficiency |
234591005 | Combined phagocytic defect |
234593008 | Classical complement pathway abnormality |
234594002 | Complement 1q deficiency |
234595001 | Complement 1q beta chain deficiency |
234596000 | Complement 1q dysfunction |
234597009 | Complement 1r deficiency |
234598004 | Complement 1s deficiency |
234599007 | Complement 2 deficiency |
234600005 | Complement 4 deficiency |
234601009 | Complement 4A deficiency |
234602002 | Complement 4B deficiency |
234603007 | Complement 3 deficiency |
234604001 | Alternative pathway deficiency |
234605000 | Factor B deficiency |
234607008 | Factor D deficiency |
234608003 | Terminal component deficiency |
234609006 | Complement 5 deficiency |
234611002 | Complement 6 deficiency |
234612009 | Complement 7 deficiency |
234613004 | Combined complement 6 and 7 deficiencies |
234614005 | Complement 8 beta chain deficiency |
234615006 | Complement 8 beta chain dysfunction |
234616007 | Complement 8 alpha-gamma deficiency |
234617003 | Complement 9 deficiency |
234618008 | Complement regulatory factor defect |
234619000 | Hereditary C1 esterase inhibitor deficiency - deficient factor |
234620006 | Hereditary C1 esterase inhibitor deficiency - dysfunctional factor |
234621005 | Factor I deficiency |
234622003 | Factor H deficiency |
234623008 | Complement 4 binding protein deficiency |
234624002 | Decay accelerating factor deficiency |
234625001 | Homologous restriction factor deficiency |
234626000 | Complement 5a inhibitor deficiency |
234627009 | Anaphylotoxin inactivator deficiency |
234628004 | Complement receptor deficiency |
234629007 | Complement receptor 1 deficiency |
234630002 | Complement receptor 3 deficiency |
234631003 | Immunodeficiency with major anomalies |
234632005 | Immunodeficiency associated with chromosomal abnormality |
234633000 | Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency |
234634006 | Chromosome 18 syndromes and antibody deficiency |
234635007 | Chromosome 22 abnormalities with hypogammaglobulinemia |
234636008 | Monosomy 22 and absence of immunoglobulin A |
234637004 | Deletion of X-chromosome and hypogammaglobulinemia |
234638009 | Microcephaly, normal intelligence and immunodeficiency |
234639001 | Triple X syndrome, epilepsy, and hypogammaglobulinemia |
234640004 | 18-p syndrome with associated immunodeficiency |
234641000 | Immunodeficiency associated with multiple organ system abnormalities |
234646005 | Graft-versus-host disease |
235009000 | Human immunodeficiency virus-associated periodontitis |
235726002 | Human immunodeficiency virus enteropathy |
236406007 | Acquired immune deficiency syndrome-related nephropathy |
236513009 | Lymphoma of kidney |
236585005 | De novo transplant disease |
23719005 | Transplantation of bone marrow |
23761004 | Hyposplenism |
237656000 | Acute splenic tumor |
237865009 | Primary amyloidosis of light chain type |
238931006 | Eosinophilic cellulitis |
239910001 | Toxic oil syndrome |
240103002 | Human immunodeficiency virus myopathy |
240531002 | African Burkitt's lymphoma |
240630008 | Hyperimmune malarious splenomegaly |
240789006 | Hepatosplenic schistosomiasis |
240790002 | Schistosomal hepatomegaly |
240791003 | Hepatic schistosomal granuloma |
240792005 | Symmer's pipe-stem fibrosis |
240793000 | Schistosomal splenomegaly |
240794006 | Splenic schistosomal giant cell lymphoma |
24159007 | Persistent lymphocytosis |
24181002 | Aplasia of thymus gland with immunodeficiency |
24419001 | Disorder of complement |
24743004 | Complement deficiency disease |
247860002 | Familial neutropenia |
24829000 | Eosinophilic ulcerative colitis |
248693006 | Chronic idiopathic neutropenia |
24974008 | Myelokathexis |
24975009 | Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
25050002 | Alpha heavy chain disease, respiratory form |
25109007 | Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome |
25167006 | Perisplenitis |
254067002 | Immuno-osseous dysplasia |
254289008 | Post-transplant neoplasia |
254290004 | Lymphoproliferative disorder following transplantation |
25472008 | Sickle cell-hemoglobin D disease |
254792006 | Proliferating angioendotheliomatosis |
25502009 | Episodic lymphocytopenia |
255101006 | Sézary disease of skin |
255102004 | Angioendotheliomatosis |
26252007 | Chronic granulomatous disease, type IIA |
262819007 | Intraparenchymal hematoma of spleen |
262821002 | Avulsion of spleen |
262823004 | Capsular tear of spleen |
2631000119108 | History of bone marrow transplant |
263661007 | Complement 5 dysfunction |
264564001 | Red pulp hamartoma |
267440005 | Monoclonal paraproteinemia |
267454002 | Acatalasemia |
267460002 | Congenital hypogammaglobulinemia |
267524009 | Constitutional aplastic anemia with malformation |
267527002 | Aplastic anemia due to drugs |
267538002 | Agranulocytopenic disorder |
267540007 | Neutropenia caused by irradiation |
267543009 | Functional disorders of polymorphonuclear neutrophils |
269295009 | Transplanted organ failure |
269476000 | Nodular lymphoma |
27254001 | Extramedullary hematopoiesis of spleen |
274905008 | Malignant lymphoma - lymphocytic, intermediate differentiation |
275523003 | Pancytopenia-dysmelia |
276576000 | Neutropenia of the small for gestational age baby |
276665006 | Congenital acquired immune deficiency syndrome |
276666007 | Congenital human immunodeficiency virus positive status syndrome |
276811008 | Gastric lymphoma |
276815004 | Lymphoma of intestine |
276836002 | Primary cerebral lymphoma |
277451006 | Part organ pancreatic transplant |
277466009 | Lymphoproliferative disorder |
277473004 | B-cell chronic lymphocytic leukemia |
277474005 | B-cell chronic lymphocytic leukemia variant |
277543005 | Malignant white blood cell disorder |
277545003 | T-cell chronic lymphocytic leukemia |
277549009 | Chronic lymphocytic prolymphocytic leukemia syndrome |
277550009 | Richter's syndrome |
277551008 | Splenic lymphoma with villous lymphocytes |
277567002 | T-cell prolymphocytic leukemia |
277568007 | Hairy cell leukemia variant |
277569004 | Large granular lymphocytic leukemia |
277570003 | Lymphoma with spill |
277571004 | B-cell acute lymphoblastic leukemia |
277572006 | Precursor B-cell acute lymphoblastic leukemia |
277573001 | Common acute lymphoblastic leukemia |
277574007 | Null cell acute lymphoblastic leukemia |
277575008 | T-cell acute lymphoblastic leukemia |
277577000 | Monoclonal gammopathy of uncertain significance |
277579002 | Light chain myeloma |
277580004 | Non-secretory myeloma |
277587001 | Juvenile chronic myeloid leukemia |
277589003 | Atypical chronic myeloid leukemia |
277597005 | Myelodysplastic syndrome with isolated del(5q) |
277601005 | Acute monoblastic leukemia |
277602003 | Acute megakaryoblastic leukemia |
277604002 | Acute eosinophilic leukemia |
277609007 | Hodgkin's disease, lymphocytic predominance - diffuse |
277610002 | Hodgkin's disease, nodular sclerosis - lymphocytic predominance |
277611003 | Hodgkin's disease, nodular sclerosis - mixed cellularity |
277612005 | Hodgkin's disease, nodular sclerosis - lymphocytic depletion |
277613000 | Cutaneous/peripheral T-cell lymphoma |
277614006 | Prethymic and thymic T-cell lymphoma/leukemia |
277615007 | Low grade B-cell lymphoma |
277616008 | Diffuse low grade B-cell lymphoma |
277617004 | High grade B-cell lymphoma |
277618009 | Follicular low grade B-cell lymphoma |
277619001 | B-cell prolymphocytic leukemia |
277622004 | Mucosa-associated lymphoma |
277623009 | Monocytoid B-cell lymphoma |
277624003 | Follicular malignant lymphoma - mixed cell type |
277625002 | Follicular malignant lymphoma - small cleaved cell |
277626001 | Diffuse high grade B-cell lymphoma |
277627005 | Nodular high grade B-cell lymphoma |
277628000 | Diffuse malignant lymphoma - large cleaved cell |
277629008 | Diffuse malignant lymphoma - large non-cleaved cell |
277632006 | Diffuse malignant lymphoma - centroblastic polymorphic |
277637000 | Large cell anaplastic lymphoma |
277641001 | Follicular malignant lymphoma - large cell |
277642008 | Low grade T-cell lymphoma |
277643003 | High grade T-cell lymphoma |
277651000 | Peripheral T-cell lymphoma - pleomorphic small cell |
277653002 | Peripheral T-cell lymphoma - pleomorphic medium and large cell |
277654008 | Enteropathy-associated T-cell lymphoma |
277664004 | Malignant lymphoma of testis |
278051002 | Malignant lymphoma of thyroid gland |
278052009 | Malignant lymphoma of breast |
278189009 | Hypergranular promyelocytic leukemia |
278453007 | Acute biphenotypic leukemia |
278484009 | Tropical pulmonary eosinophilia |
281388009 | Human immunodeficiency virus-related sclerosing cholangitis |
28399005 | Tuberculosis of spleen |
285420006 | Immunoglobulin A myeloma |
285421005 | Immunoglobulin G myeloma |
285422003 | Immunoglobulin D myeloma |
285423008 | Immunoglobulin A monoclonal gammopathy of uncertain significance |
285424002 | Immunoglobulin G monoclonal gammopathy of uncertain significance |
285426000 | Immunoglobulin M monoclonal gammopathy of uncertain significance |
285428004 | Immunoglobulin D monoclonal gammopathy of uncertain significance |
285430002 | Light chain monoclonal gammopathy of uncertain significance |
285615003 | Metastasis to spleen of unknown primary |
285769009 | Acute promyelocytic leukemia - hypogranular variant |
285776004 | Intermediate grade B-cell lymphoma |
285839005 | Acute myelomonocytic leukemia - eosinophilic variant |
287239002 | Thymus transplantation |
288327009 | Granulation anomaly |
289317009 | Granulocyte granule deficiency |
28975000 | Constitutional aplastic anemia |
29120000 | Eosinophilic colitis |
29260007 | Immunoglobulin A deficiency |
29272001 | Chronic granulomatous disease, type I |
29789008 | Monocytic leukemoid reaction |
2990008 | Lymphocytic leukemoid reaction |
300564004 | Spleen absent |
302841002 | Malignant lymphoma - small lymphocytic |
302842009 | Diffuse malignant lymphoma - centroblastic |
302845006 | Nodular malignant lymphoma, lymphocytic - well differentiated |
302848008 | Nodular malignant lymphoma, lymphocytic - intermediate differentiation |
302855005 | Subacute leukemia |
302856006 | Aleukemic leukemia |
302874002 | Phagocytic cell dysfunction |
302961007 | Hereditary splenic hypoplasia |
303011007 | Neutropenic disorder |
303017006 | Malignant lymphoma, convoluted cell type |
303055001 | Malignant lymphoma, follicular center cell |
303056000 | Malignant lymphoma, follicular center cell, cleaved |
303057009 | Malignant lymphoma, follicular center cell, non-cleaved |
304576008 | Metaphyseal chondrodysplasia, McKusick type with associated immunodeficiency |
30575002 | Fanconi's anemia |
306058006 | Aplastic anemia |
307340003 | Monosomy 7 syndrome |
307341004 | Atypical hairy cell leukemia |
307592006 | Basophilic leukemia |
307617006 | Neutrophilic leukemia |
307622006 | Prolymphocytic lymphosarcoma |
307623001 | Malignant lymphoma - lymphoplasmacytic |
307624007 | Diffuse malignant lymphoma - centroblastic-centrocytic |
307625008 | Malignant lymphoma - centrocytic |
307633009 | Hodgkin's disease, lymphocytic depletion, diffuse fibrosis |
307634003 | Hodgkin's disease, lymphocytic depletion, reticular type |
307635002 | Hodgkin's disease, nodular sclerosis - cellular phase |
307636001 | Malignant lymphoma, mixed lymphocytic-histiocytic, nodular |
307637005 | Malignant lymphoma, centroblastic-centrocytic, follicular |
307646004 | Malignant lymphoma, lymphocytic, poorly differentiated, nodular |
307647008 | Malignant lymphoma, centroblastic type, follicular |
307649006 | Microglioma |
307651005 | Myelosclerosis with myeloid metaplasia |
308121000 | Follicular non-Hodgkin's lymphoma |
30981000 | Secondary eosinophilia |
31047003 | Lymphomatoid papulosis |
313039003 | Solid organ transplant |
31323000 | Severe combined immunodeficiency disease |
313427003 | Lambda light chain myeloma |
314118002 | Laparoscopic total splenectomy |
315019000 | Human immunodeficiency virus infection with aseptic meningitis |
317226009 | Granulocytosis |
319171004 | Qualitative abnormality of granulocyte |
320150004 | Idiopathic eosinophilia |
32092008 | Toxic neutropenia |
3239007 | Lymphocyte disorder |
33479006 | Distal subtotal pancreatectomy with splenectomy and pancreaticojejunostomy |
3439009 | Severe combined immunodeficiency due to absent peripheral T cell maturation |
34916006 | Neutrophil motility disorder |
350353007 | De Vaal's syndrome |
350951000119101 | B-cell lymphoma of intra-abdominal lymph nodes |
351211000119104 | B-cell lymphoma of lymph nodes of multiple sites |
351287008 | Reticular dysgenesis with congenital aleukocytosis |
352251000119109 | Small lymphocytic B-cell lymphoma of lymph nodes of multiple sites |
352411000119109 | Small lymphocytic B-cell lymphoma of intra-abdominal lymph nodes |
352791000119108 | Non-Hodgkin's lymphoma of lymph nodes of multiple sites |
35434009 | Sickle cell-hemoglobin C disease |
354851000119101 | Follicular non-Hodgkin's lymphoma of lymph nodes of multiple sites |
359631009 | Acute myeloid leukemia, minimal differentiation, FAB M0 |
359640008 | Acute myeloid leukemia without maturation, FAB M1 |
359648001 | Acute myeloid leukemia with maturation, FAB M2 |
36070007 | Wiskott-Aldrich syndrome |
361195001 | Pulmonary fibroplasia |
36138009 | Congenital immunodeficiency disease |
362993009 | Autosomal recessive severe combined immunodeficiency disease |
363009005 | Complement component deficiency |
363040003 | Congenital immunodeficiency involving the hematopoietic system |
363138005 | Hereditary disorder of immune system |
363265005 | Predominant humoral immune deficiency |
363499005 | Malignant tumor of spleen |
36472007 | Sickle cell-thalassemia disease |
36752001 | Congenital splenomegaly |
36760000 | Hepatosplenomegaly |
36980009 | Severe combined immunodeficiency due to absent adenosine deaminase |
371012000 | Acute lymphoblastic leukemia, transitional pre-B-cell |
371134001 | Malignant lymphoma, large cell, polymorphous, immunoblastic |
373168002 | Reticulosarcoma |
373604002 | Light chain deposition disease |
37465004 | Plasmacytosis |
37548006 | Hypopigmentation-immunodeficiency disease |
378841000000102 | Allograft of bone marrow from unmatched unrelated donor |
38064006 | Reactive monocytosis |
38096003 | Functional asplenia |
387759001 | Chronic granulomatous disease |
38970002 | Doan-Wright syndrome |
3902000 | Non dose-related drug-induced neutropenia |
396330006 | Celiac crisis |
396331005 | Celiac disease |
39674000 | Familial C3B inhibitor deficiency syndrome |
397007003 | Mast cell disorder |
397016004 | Systemic mast cell disease |
397763006 | Human immunodeficiency virus encephalopathy |
398055000 | T-lymphocyte deficiency |
398250003 | Familial hemophagocytic lymphohistiocytosis |
398329009 | Human immunodeficiency virus encephalitis |
398623004 | Refractory anemia with excess blasts |
400001003 | Primary cutaneous lymphoma |
400122007 | Primary cutaneous T-cell lymphoma |
40145002 | Congenital neutrophil actin dysfunction |
40197009 | Chronic granulomatous disease, type IA |
402356004 | Chronic graft-versus-host disease |
402357008 | Lichenoid chronic graft-versus-host disease |
402358003 | Sclerodermoid chronic graft-versus-host disease |
402360001 | Materno-fetal graft-versus-host disease |
402483002 | Immunodeficiency with multicarboxylase deficiency |
402791005 | B-lymphocyte immunodeficiency |
402792003 | T-lymphocyte immunodeficiency |
402793008 | Heritable disorder of neutrophil production |
402794002 | Heritable disorder of neutrophil function |
402880009 | Primary cutaneous large T-cell lymphoma |
402881008 | Primary cutaneous B-cell lymphoma |
402882001 | Hodgkin's disease affecting skin |
402901009 | Oral hairy leukoplakia associated with human immunodeficiency virus disease |
403735006 | Eosinophilia-myalgia syndrome from tryptophan |
403835002 | X-linked hyper-immunoglobulin M syndrome |
403836001 | Autosomal recessive hyperimmunoglobulin M syndrome |
403837005 | Wiskott-Aldrich autosomal dominant variant syndrome |
403838000 | Jung syndrome |
403839008 | Siccardi syndrome |
404103007 | Lymphomatoid papulosis type A (CD-30 positive type) |
404104001 | Lymphomatoid papulosis type B - mycosis fungoides-like |
404105000 | Lymphomatoid papulosis type C (anaplastic large-cell lymphoma-like) |
404106004 | Lymphomatoid papulosis with Hodgkin's disease |
404107008 | Patch/plaque stage mycosis fungoides |
404108003 | Poikilodermatous mycosis fungoides |
404109006 | Follicular mucinosis type mycosis fungoides |
404110001 | Hypomelanotic mycosis fungoides |
404111002 | Lymphomatoid papulosis-associated mycosis fungoides |
404112009 | Granulomatous mycosis fungoides |
404113004 | Tumor stage mycosis fungoides |
404114005 | Erythrodermic mycosis fungoides |
404115006 | Bullous mycosis fungoides |
404116007 | Mycosis fungoides with systemic infiltration |
404117003 | Spongiotic mycosis fungoides |
404118008 | Syringotropic mycosis fungoides |
404119000 | Pagetoid reticulosis |
404120006 | Localized pagetoid reticulosis |
404121005 | Generalized pagetoid reticulosis |
404122003 | Leukemic infiltration of skin (chronic T-cell lymphocytic leukemia) |
404123008 | Leukemic infiltration of skin (T-cell prolymphocytic leukemia) |
404124002 | Leukemic infiltration of skin (T-cell lymphoblastic leukemia) |
404125001 | CD-30 positive anaplastic large T-cell cutaneous lymphoma |
404126000 | CD-30 positive pleomorphic large T-cell cutaneous lymphoma |
404127009 | CD-30 positive T-immunoblastic cutaneous lymphoma |
404128004 | CD-30 negative cutaneous T-cell lymphoma |
404129007 | CD-30 negative anaplastic large T-cell cutaneous lymphoma |
404130002 | CD-30 negative pleomorphic large T-cell cutaneous lymphoma |
404131003 | CD-30 negative T-immunoblastic cutaneous lymphoma |
404132005 | Pleomorphic small/medium-sized cell cutaneous T-cell lymphoma |
404133000 | Subcutaneous panniculitic cutaneous T-cell lymphoma |
404134006 | Anaplastic large T-cell systemic malignant lymphoma |
404135007 | Angiocentric natural killer/T-cell malignant lymphoma involving skin |
404136008 | Aggressive natural killer-cell leukemia involving skin |
404137004 | Precursor B-cell lymphoblastic lymphoma involving skin |
404138009 | Small lymphocytic B-cell lymphoma involving skin |
404139001 | Leukemic infiltration of skin in hairy-cell leukemia |
404140004 | Primary cutaneous marginal zone B-cell lymphoma |
404141000 | Primary cutaneous immunocytoma |
404142007 | Primary cutaneous plasmacytoma |
404143002 | Primary cutaneous follicular center B-cell lymphoma |
404144008 | Primary cutaneous diffuse large cell B-cell lymphoma |
404145009 | Primary cutaneous anaplastic large cell B-cell lymphoma |
404146005 | Primary cutaneous diffuse large cell B-cell lymphoma of the leg |
404147001 | Follicular center B-cell lymphoma (nodal/systemic with skin involvement) |
404148006 | Diffuse large B-cell lymphoma (nodal/systemic with skin involvement) |
404149003 | Lymphoplasmacytic B-cell lymphoma, nodal/systemic with skin involvement |
404150003 | Mantle cell B-cell lymphoma (nodal/systemic with skin involvement) |
404151004 | Leukemic infiltration of skin in myeloid leukemia |
404152006 | Leukemic infiltration of skin in acute myeloid leukemia |
404153001 | Leukemic infiltration of skin in chronic myeloid leukemia |
404154007 | Leukemic infiltration of skin in monocytic leukemia |
404157000 | Specific skin infiltration in Hodgkin's disease |
405631006 | Pediatric human immunodeficiency virus infection |
406565005 | CD4 T lymphocyte deficiency |
40780007 | Human immunodeficiency virus I infection |
409089005 | Febrile neutropenia |
413389003 | Accelerated phase chronic myeloid leukemia |
413441006 | Acute monocytic leukemia, FAB M5b |
413442004 | Acute monocytic/monoblastic leukemia |
413537009 | Angioimmunoblastic T-cell lymphoma |
413565006 | Aplastic anemia associated with metabolic alteration |
413566007 | Aplastic anemia associated with pancreatitis |
413567003 | Aplastic anemia associated with pregnancy |
413587002 | Smoldering myeloma |
413656006 | Blastic phase chronic myeloid leukemia |
413834006 | Chronic disease of immune function |
413842007 | Chronic myeloid leukemia in lymphoid blast crisis |
413843002 | Chronic myeloid leukemia in myeloid blast crisis |
413847001 | Chronic phase chronic myeloid leukemia |
414029004 | Disorder of immune function |
414166008 | Extranodal natural killer/T-cell lymphoma, nasal type |
414376003 | Hairy leukoplakia of tongue associated with human immunodeficiency virus disease |
414395005 | Hereditary white blood cell disorder |
414553000 | Kappa light chain myeloma |
414604009 | Leukoplakia of tongue associated with human immunodeficiency virus disease |
414780005 | Mucosa-associated lymphoid tissue lymphoma of orbit |
414785000 | Multiple solitary plasmacytomas |
414850009 | Neutrophilia |
415005004 | Panleukopenia |
415112005 | Plasmacytoma |
415283002 | Refractory anemia with excess blasts-1 |
415284008 | Refractory anemia with excess blasts-2 |
415287001 | Relapsing chronic myeloid leukemia |
416180004 | Hemoglobin SS disease without crisis |
416214006 | Sickle cell-hemoglobin D disease without crisis |
416290001 | Hemoglobin S sickling disorder without crisis |
416484003 | Sickle cell-hemoglobin E disease with crisis |
416491000 | Immune recovery uveitis |
416638004 | Sickle cell-hemoglobin E disease without crisis |
416729007 | Neutropenia associated with acquired immunodeficiency syndrome |
416826005 | Sickle cell-thalassemia disease with crisis |
417048006 | Sickle cell-thalassemia disease without crisis |
417167007 | Immunoglobulin deficiency |
417279003 | Hemoglobin S sickling disorder with crisis |
417357006 | Sickling disorder due to hemoglobin S |
417425009 | Hemoglobin SS disease with crisis |
417517009 | Sickle cell-hemoglobin C disease with crisis |
417672002 | Granulocytopenic disorder |
417683006 | Sickle cell-hemoglobin C disease without crisis |
417748003 | Sickle cell-hemoglobin D disease with crisis |
41814009 | Neutropenia with dysgranulopoiesis |
420403001 | Pneumocystosis associated with acquired immunodeficiency syndrome |
420519005 | Malignant lymphoma of the eye region |
420544002 | Bacterial pneumonia associated with acquired immunodeficiency syndrome |
420787001 | Pneumococcal pneumonia associated with acquired immunodeficiency syndrome |
420788006 | Intraocular non-Hodgkin malignant lymphoma |
420818005 | Mycobacteriosis associated with acquired immunodeficiency syndrome |
421047005 | Candidiasis of lung associated with acquired immunodeficiency syndrome |
421102007 | Aplastic anemia associated with acquired immunodeficiency syndrome |
421246008 | Precursor T-cell lymphoblastic lymphoma |
421312009 | Agranulocytosis associated with acquired immunodeficiency syndrome |
421460008 | Retinopathy associated with acquired immunodeficiency syndrome |
421508002 | Viral pneumonia associated with acquired immunodeficiency syndrome |
421671002 | Pneumonia associated with acquired immunodeficiency syndrome |
422003001 | Cachexia associated with acquired immunodeficiency syndrome |
422853008 | Lymphoma of retroperitoneal space |
423294001 | Idiopathic hypereosinophilic syndrome |
423486005 | Disseminated eosinophilic collagen disease |
425333006 | Myeloproliferative disorder |
425616008 | Transplantation of ileum |
425657001 | Osteosclerotic myeloma |
425688002 | Philadelphia chromosome-positive acute lymphoblastic leukemia |
425749006 | Subacute myeloid leukemia in remission |
425835006 | Disorder of immune reconstitution |
425869007 | Acute promyelocytic leukemia, FAB M3, in remission |
425941003 | Precursor B-cell acute lymphoblastic leukemia in remission |
426071002 | Hodgkin's disease in remission |
426124006 | Acute myeloid leukemia with maturation, FAB M2, in remission |
426202004 | Immune reconstitution syndrome |
426217000 | Aleukemic leukemia in remission |
426248008 | Aleukemic lymphoid leukemia in remission |
426336007 | Solitary osseous myeloma |
426370008 | Subacute lymphoid leukemia in remission |
426425001 | Allograft of bone marrow from sibling donor |
426463009 | Allotransplantation of ileum |
426598005 | Amyloid light-chain nephropathy |
426642002 | Erythroleukemia, FAB M6 in remission |
426768001 | Engraftment syndrome |
426800001 | Febrile granulocytopenia |
426885008 | Hodgkin's disease, lymphocytic depletion of lymph nodes of head |
426984008 | Allotransplantation of thymus gland |
427056005 | Subacute leukemia in remission |
427141003 | Malignant lymphoma in remission |
427167008 | Hereditary angioedema with normal C1 esterase inhibitor activity |
427245000 | Febrile leukopenia |
427423003 | Allograft of bone marrow from matched unrelated donor |
427642009 | T-cell acute lymphoblastic leukemia in remission |
427658007 | Acute myelomonocytic leukemia, FAB M4, in remission |
428198008 | Transplantation of hepatocytes |
429054002 | Disorder related to transplantation |
429490004 | Disorder affecting transplanted structure |
430338009 | Smoldering chronic lymphocytic leukemia |
430478003 | Macrophage activation syndrome |
430822009 | Basophilic leukemoid reaction |
431456004 | Accelerated rejection of bone marrow transplant |
431505005 | Rejection of intestine transplant |
431506006 | Rejection of pancreas transplant |
431862001 | Acute rejection of bone marrow transplant |
431953002 | Chronic rejection of bone marrow transplant |
432782005 | Hyperacute rejection of bone marrow transplant |
43355006 | Eosinopenia |
433592008 | Acute rejection of pancreas transplant |
433600001 | Hyperacute rejection of intestine transplant |
433804007 | Accelerated rejection of intestine transplant |
433809002 | Accelerated rejection of pancreas transplant |
434202008 | Hyperacute rejection of pancreas transplant |
434238001 | Acute rejection of intestine transplant |
434270001 | Chronic rejection of intestine transplant |
434271002 | Chronic rejection of pancreas transplant |
43858000 | Secondary aplastic anemia |
440206000 | Hemoglobin SS disease with vasoocclusive crisis |
440422002 | Asymptomatic multiple myeloma |
441313008 | Indolent multiple myeloma |
441482006 | History of sickle cell anemia |
441559006 | Mantle cell lymphoma of spleen |
441962003 | Large cell lymphoma of intrapelvic lymph nodes |
442360003 | Calcification of spleen |
442459007 | Combined immunodeficiency disease |
442537007 | Non-Hodgkin lymphoma associated with Human immunodeficiency virus infection |
442557006 | Grafting of bone marrow using allograft from unmatched unrelated donor |
44306006 | T lymphocyte disorder |
4434006 | Bloom syndrome |
443487006 | Mantle cell lymphoma |
444108000 | Acute sickle cell splenic sequestration crisis |
444547006 | Graft versus host disease of skin |
444597005 | Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue of stomach |
444910004 | Primary mediastinal (thymic) large B-cell lymphoma |
444911000 | Acute myeloid leukemia with t(9:11)(p22;q23); MLLT3-MLL |
445105005 | Blastic plasmacytoid dendritic cell neoplasm |
445227008 | Juvenile myelomonocytic leukemia |
445269007 | Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue |
445406001 | Hepatosplenic T-cell lymphoma |
445448008 | Acute myeloid leukemia with myelodysplasia-related changes |
445738007 | Myelodysplastic/myeloproliferative disease |
445757003 | Allogeneic bone marrow transplantation without purging |
446253009 | Allogeneic bone marrow transplantation with purging |
446643000 | Sarcoma of dendritic cells (accessory cells) |
447100004 | Marginal zone lymphoma |
447596005 | Myelodysplastic/myeloproliferative neoplasm, unclassifiable |
447656001 | Lymphoma of pylorus of stomach |
447658000 | Lymphoma of fundus of stomach |
447766003 | Lymphoma of pyloric antrum of stomach |
447805007 | Lymphoma of greater curvature of stomach |
447806008 | Lymphoma of cardia of stomach |
447989004 | Non-Hodgkin's lymphoma of extranodal site |
448212009 | Anaplastic lymphoma kinase negative anaplastic large cell lymphoma |
448213004 | Diffuse non-Hodgkin's lymphoma of prostate |
448217003 | Follicular non-Hodgkin's lymphoma of prostate |
448220006 | Non-Hodgkin's lymphoma of bone |
448231003 | Follicular non-Hodgkin's lymphoma of nose |
448254007 | Non-Hodgkin's lymphoma of central nervous system |
448269008 | Lymphoma of lesser curvature of stomach |
448317000 | Follicular non-Hodgkin's lymphoma of soft tissue |
448319002 | Diffuse non-Hodgkin's lymphoma of nasopharynx |
448354009 | Non-Hodgkin's lymphoma of intestine |
448371005 | Non-Hodgkin's lymphoma of nasopharynx |
448372003 | Non-Hodgkin's lymphoma of lung |
448376000 | Non-Hodgkin's lymphoma of ovary |
448384001 | Non-Hodgkin's lymphoma of nose |
448386004 | Non-Hodgkin's lymphoma of oral cavity |
448387008 | Non-Hodgkin's lymphoma of testis |
448447004 | Non-Hodgkin's lymphoma of skin |
448465000 | Diffuse non-Hodgkin's lymphoma of testis |
448468003 | Diffuse non-Hodgkin's lymphoma of oral cavity |
448553002 | Lymphoma of pelvis |
448555009 | Lymphoma of body of stomach |
448560008 | Diffuse non-Hodgkin's lymphoma of extranodal site |
448561007 | Follicular non-Hodgkin's lymphoma of extranodal site |
448607004 | Diffuse non-Hodgkin's lymphoma of uterine cervix |
448609001 | Diffuse non-Hodgkin's lymphoma of ovary |
448663003 | Diffuse non-Hodgkin's lymphoma of stomach |
448666006 | Follicular non-Hodgkin's lymphoma of bone |
448672006 | Follicular non-Hodgkin's lymphoma of lung |
448709005 | Non-Hodgkin's lymphoma of stomach |
448738008 | Non-Hodgkin's lymphoma of soft tissue |
448774004 | Non-Hodgkin's lymphoma of uterine cervix |
448865007 | Follicular non-Hodgkin's lymphoma of skin |
448867004 | Diffuse non-Hodgkin's lymphoma of lung |
448995000 | Follicular non-Hodgkin's lymphoma of central nervous system |
449053004 | Lymphoma of lower esophagus |
449058008 | Follicular non-Hodgkin's lymphoma of tonsil |
449059000 | Follicular non-Hodgkin's lymphoma of uterine cervix |
449063007 | Follicular non-Hodgkin's lymphoma of oral cavity |
449065000 | Diffuse non-Hodgkin's lymphoma of nose |
449072004 | Lymphoma of gastrointestinal tract |
449074003 | Lymphoma of small intestine |
449075002 | Lymphoma of cardioesophageal junction |
449108003 | Philadelphia chromosome positive chronic myelogenous leukemia |
449173006 | Diffuse non-Hodgkin's lymphoma of tonsil |
449176003 | Diffuse non-Hodgkin's lymphoma of intestine |
449177007 | Diffuse non-Hodgkin's lymphoma of bone |
449187006 | Kappa light chain deficiency |
449216004 | Diffuse non-Hodgkin's lymphoma of soft tissue |
449217008 | Diffuse non-Hodgkin's lymphoma of skin |
449218003 | Lymphoma of sigmoid colon |
449219006 | Follicular non-Hodgkin's lymphoma of nasopharynx |
449220000 | Diffuse follicle center lymphoma |
449221001 | Diffuse non-Hodgkin's lymphoma of central nervous system |
449222008 | Follicular non-Hodgkin's lymphoma of stomach |
449292003 | Non-Hodgkin's lymphoma of tonsil |
449307001 | Follicular non-Hodgkin's lymphoma of ovary |
449318001 | Non-Hodgkin's lymphoma of prostate |
449384005 | Lambda light chain deficiency |
449386007 | Philadelphia chromosome negative chronic myelogenous leukemia |
44940001 | Adenosine deaminase deficiency |
449418000 | Follicular non-Hodgkin's lymphoma of testis |
449419008 | Follicular non-Hodgkin's lymphoma of intestine |
449784008 | Diffuse infiltrative lymphocytosis syndrome |
449853003 | Interleukin-12 deficiency |
45259000 | Celiac infantilism |
45390000 | Severe combined immunodeficiency due to absent interleukin-2 production |
45841007 | Kappa light chain disease |
46280001 | Autologous bone marrow transplant with purging |
46288008 | Payr's syndrome |
46359005 | Neutropenia associated with infectious disease |
46760003 | Estren-Dameshek anemia |
47024008 | Sickle cell-hemoglobin E disease |
47144000 | Acute neutrophilia |
47318007 | Drug-induced neutropenia |
47516005 | Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
47986005 | Genetic anomaly of leukocyte |
48119005 | Dysplasia of thymus gland with immunodeficiency |
48794007 | Human immunodeficiency virus infection with infectious mononucleosis-like syndrome |
48813009 | Lymphocytopenia |
49555001 | Severe combined immunodeficiency due to absent T cell receptor |
50220002 | Cellular immunologic aplastic anemia |
50926003 | Job's syndrome |
51319002 | Light chain disease |
51577008 | Wilson-Mikity syndrome |
52064007 | Biclonal gammopathy |
52079000 | Congenital human immunodeficiency virus infection |
52967002 | Myelofibrosis |
54097007 | White blood cell disorder |
55444004 | Transient neonatal neutropenia |
55602000 | Nezelof's syndrome |
55907008 | Acquired aplastic anemia |
56118002 | Congenital syphilitic splenomegaly |
56338005 | Splenic fibrosis |
56478004 | Leukemoid reaction |
56918001 | Dose-related drug-induced neutropenia |
58034007 | Congenital hypergammaglobulinemia |
58381000 | Hypersplenism |
58390007 | Allogeneic bone marrow transplantation |
58606001 | Primary immune deficiency disorder |
58639003 | Doan-Wiseman syndrome |
58648008 | Benign monoclonal gammopathy |
5876000 | Acquired pancytopenia |
58776007 | Autologous bone marrow transplant |
58961005 | Lethal midline granuloma |
60194009 | Distal subtotal pancreatectomy with splenectomy |
60620005 | Epsilon heavy chain disease |
60743005 | Purine-nucleoside phosphorylase deficiency |
61291000119103 | Disorder of central nervous system co-occurrent and due to acute lymphoid leukemia in remission |
61301000119102 | Disorder of central nervous system co-occurrent and due to acute lymphoid leukemia |
61493004 | Mu heavy chain disease |
61535006 | Transplantation of spleen |
61596005 | Heterophil-positive mononucleosis syndrome |
61715008 | Celiac disease with diffuse intestinal ulceration |
61777009 | Thalassemia-hemoglobin C disease |
62438007 | Transplantation of pancreas |
63484008 | Drug-induced neutrophilia |
64249002 | Allergic eosinophilia |
64936001 | Löffler's syndrome |
65230006 | Heterophil-negative mononucleosis syndrome |
65623009 | Immune neutropenia |
65880007 | X-linked agammaglobulinemia |
66876008 | Lambda light chain disease |
67023009 | Lymphocytosis |
67562009 | Heterotransplant of pancreas |
68504005 | Ataxia-telangiectasia syndrome |
68712004 | Lymphocytic hypoplasia |
68979007 | Heavy chain disease |
697919000 | Pulmonary hypertension due to post-splenectomy hematological disorder |
698303004 | Awaiting transplantation of bone marrow |
698362007 | History of transplantation of pancreas |
698367001 | History of transplantation of intestine |
698646006 | Acute monoblastic leukemia in remission |
699657009 | Hepatosplenic gamma-delta cell lymphoma |
699818003 | T-cell large granular lymphocytic leukemia |
699861000 | Familial granulomatous inflammatory arthritis, dermatitis and uveitis |
699869003 | Interleukin-1 receptor-associated kinase 4 deficiency |
700050004 | Overwhelming infection in asplenic patient |
700051000 | Sepsis in asplenic subject |
700052007 | Post-splenectomy sepsis |
702444009 | Autoimmune lymphoproliferative syndrome |
702446006 | Core binding factor acute myeloid leukemia |
702476004 | Therapy-related myelodysplastic syndrome |
702624008 | Aplasia of spleen |
702785000 | Large cell anaplastic lymphoma T cell and Null cell type |
702786004 | Follicular non-Hodgkin's lymphoma diffuse follicle center sub-type grade 1 |
702977001 | Follicular non-Hodgkin's lymphoma diffuse follicle center cell sub-type grade 2 |
703387000 | Acute myeloid leukemia with normal karyotype |
70349007 | Pseudoneutrophilia |
703523004 | Spondyloenchondrodysplasia with immune dysregulation |
703525006 | Anhidrotic ectodermal dysplasia with immune deficiency |
703538003 | Mannose-binding lectin deficiency |
703626001 | Anaplastic large cell lymphoma, T/Null cell, primary systemic type |
705061009 | Childhood myelodysplastic syndrome |
707147002 | Asplenia |
707152007 | Phagocytic immunodeficiency |
709465004 | Periodontitis co-occurrent with Chédiak-Higashi syndrome |
709471005 | Periodontitis co-occurrent with leukemia |
709535007 | Periodontitis co-occurrent with infantile genetic agranulocytosis |
70958007 | Plasma cell hyperplasia of bone marrow |
709608008 | Periodontitis co-occurrent with acquired neutropenia |
710735009 | Periodontitis co-occurrent with leukocyte adhesion deficiency |
710926008 | Periodontitis co-occurrent with familial neutropenia |
710927004 | Periodontitis co-occurrent with cyclical neutropenia |
711160007 | Eosinophil peroxidase deficiency |
711164003 | STING-associated vasculopathy with onset in infancy |
711407000 | Thrombocytopathy, asplenia and miosis |
711480000 | Activated PI3K-delta syndrome |
713260006 | Subacute adenoviral encephalitis co-occurrent with human immunodeficiency virus infection |
713275003 | Splenomegaly co-occurrent with human immunodeficiency virus infection |
713278001 | Neuralgia co-occurrent with human immunodeficiency virus infection |
713297001 | Candidiasis of esophagus co-occurrent with human immunodeficiency virus infection |
713298006 | Heart disease co-occurrent with human immunodeficiency virus infection |
713299003 | Disorder of eye proper co-occurrent with human immunodeficiency virus infection |
713300006 | Disorder of gastrointestinal tract co-occurrent with human immunodeficiency virus infection |
713316008 | Eruption of skin co-occurrent with human immunodeficiency virus infection |
713318009 | Myocarditis co-occurrent with human immunodeficiency virus infection |
713320007 | Radiculitis co-occurrent with human immunodeficiency virus infection |
713325002 | Primary cerebral lymphoma co-occurrent with human immunodeficiency virus infection |
713339002 | Infection caused by Strongyloides co-occurrent with human immunodeficiency virus infection |
713340000 | Disorder of skin co-occurrent with human immunodeficiency virus infection |
713341001 | Myelitis co-occurrent with human immunodeficiency virus infection |
713342008 | Infection caused by Salmonella co-occurrent with human immunodeficiency virus infection |
713349004 | Anemia co-occurrent with human immunodeficiency virus infection |
713444005 | Hemophagocytic syndrome co-occurrent with human immunodeficiency virus infection |
713445006 | Disseminated infection caused by Strongyloides co-occurrent with human immunodeficiency virus infection |
713446007 | Chronic infection caused by herpes simplex virus co-occurrent with human immunodeficiency virus infection |
713483007 | Reticulosarcoma co-occurrent with human immunodeficiency virus infection |
713484001 | Disorder of respiratory system co-occurrent with human immunodeficiency virus infection |
713487008 | Progressive multifocal leukoencephalopathy co-occurrent with human immunodeficiency virus infection |
713488003 | Presenile dementia co-occurrent with human immunodeficiency virus infection |
713489006 | Polyneuropathy co-occurrent with human immunodeficiency virus infection |
713490002 | Infection caused by Pneumocystis co-occurrent with human immunodeficiency virus infection |
713491003 | Organic brain syndrome co-occurrent with human immunodeficiency virus infection |
713497004 | Candidiasis of mouth co-occurrent with human immunodeficiency virus infection |
713503007 | Disorder of spinal cord co-occurrent with human immunodeficiency virus infection |
713504001 | Disorder of kidney co-occurrent with human immunodeficiency virus infection |
713505000 | Gastrointestinal malabsorption syndrome co-occurrent with human immunodeficiency virus infection |
713506004 | Neuritis co-occurrent with human immunodeficiency virus infection |
713507008 | Lymphadenopathy co-occurrent with human immunodeficiency virus infection |
713508003 | Aplastic anemia co-occurrent with human immunodeficiency virus infection |
713510001 | Enlargement of liver co-occurrent with human immunodeficiency virus infection |
713511002 | Acute endocarditis co-occurrent with human immunodeficiency virus infection |
713516007 | Primary effusion lymphoma |
713523008 | Cardiomyopathy co-occurrent with human immunodeficiency virus infection |
713526000 | Recurrent bacterial pneumonia co-occurrent with human immunodeficiency virus infection |
713527009 | Disorder of peripheral nervous system co-occurrent with human immunodeficiency virus infection |
713530002 | Agranulocytosis co-occurrent with human immunodeficiency virus infection |
713531003 | Visual impairment co-occurrent with human immunodeficiency virus infection |
713532005 | Infective arthritis co-occurrent with human immunodeficiency virus infection |
713533000 | Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection |
713543002 | Demyelinating disease of central nervous system co-occurrent with human immunodeficiency virus infection |
713544008 | Bacterial pneumonia co-occurrent with human immunodeficiency virus infection |
713545009 | Infection caused by Nocardia co-occurrent with human immunodeficiency virus infection |
713546005 | Isosporiasis co-occurrent with human immunodeficiency virus infection |
713570009 | Infectious gastroenteritis co-occurrent with human immunodeficiency virus infection |
713571008 | Disorder of central nervous system co-occurrent with human immunodeficiency virus infection |
713572001 | Malignant neoplastic disease co-occurrent with human immunodeficiency virus infection |
713695001 | Nephrotic syndrome co-occurrent with human immunodeficiency virus infection |
713696000 | Renal failure syndrome co-occurrent with human immunodeficiency virus infection |
713718006 | Diffuse non-Hodgkin immunoblastic lymphoma co-occurrent with human immunodeficiency virus infection |
713722001 | Infection caused by Cytomegalovirus co-occurrent with human immunodeficiency virus infection |
713729005 | Infection caused by Coccidia co-occurrent with human immunodeficiency virus infection |
713730000 | Infection caused by herpes simplex virus co-occurrent with human immunodeficiency virus infection |
713731001 | Pyrexia of unknown origin co-occurrent with human immunodeficiency virus infection |
713732008 | Infection caused by Aspergillus co-occurrent with human immunodeficiency virus infection |
713733003 | Infection caused by herpes zoster virus co-occurrent with human immunodeficiency virus infection |
713734009 | Infection caused by Dermatophyte co-occurrent with human immunodeficiency virus infection |
713742005 | Human immunodeficiency virus antibody positive |
713844000 | Dementia co-occurrent with human immunodeficiency virus infection |
713845004 | Infection caused by Cryptosporidium co-occurrent with human immunodeficiency virus infection |
713880000 | Opportunistic mycosis co-occurrent with human immunodeficiency virus infection |
713881001 | Infection caused by Microsporidia co-occurrent with human immunodeficiency virus infection |
713887002 | Focal segmental glomerulosclerosis co-occurrent with human immunodeficiency virus infection |
713897006 | Burkitt lymphoma co-occurrent with human immunodeficiency virus infection |
713964006 | Multidermatomal infection caused by Herpes zoster co-occurrent with human immunodeficiency virus infection |
713967004 | Disseminated atypical infection caused by Mycobacterium co-occurrent with human immunodeficiency virus infection |
714083007 | Recurrent salmonella sepsis co-occurrent with human immunodeficiency virus infection |
714251006 | Philadelphia chromosome-negative precursor B-cell acute lymphoblastic leukemia |
71436005 | Lazy leukocyte syndrome |
714463003 | Primary effusion lymphoma co-occurrent with infection caused by Human herpesvirus 8 |
714464009 | Immune reconstitution inflammatory syndrome caused by human immunodeficiency virus infection |
715950008 | Anaplastic lymphoma kinase positive large B-cell lymphoma |
715982006 | Severe combined immunodeficiency due to deoxyribonucleic acid cross-link repair protein 1c deficiency |
71610005 | Neutrophilic leukemoid reaction |
716192009 | Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome |
716198008 | Growth delay with hydrocephalus and lung hypoplasia syndrome |
716378008 | Combined immunodeficiency due to Zeta-chain associated protein kinase 70 deficiency |
716655008 | Aggressive systemic mastocytosis |
716788007 | Epstein-Barr virus positive diffuse large B-cell lymphoma of elderly |
716869006 | Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency |
716871006 | Severe combined immunodeficiency due to deoxyribonucleic acid dependent protein kinase catalytic subunit deficiency |
71692003 | Leukoerythroblastotic reaction |
717156002 | Biliary atresia with splenic malformation syndrome |
717780007 | Monoclonal B-cell lymphocytosis |
717811007 | Combined immunodeficiency due to calcium release activated calcium channel dysfunction |
718107000 | Severe combined immunodeficiency T-cell negative B-cell positive due to janus kinase-3 deficiency |
718200007 | Primary pulmonary lymphoma |
718230004 | Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency |
718232007 | Pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 |
718614004 | Telangiectasia, erythrocytosis, monoclonal gammopathy, perinephric fluid collections and intrapulmonary shunting syndrome |
718717004 | Primary immunodeficiency syndrome due to p14 deficiency |
718882006 | X-linked severe congenital neutropenia |
719019000 | WT limb blood syndrome |
71904008 | Severe combined immunodeficiency due to absent class II human leukocyte antigens |
719156006 | X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome |
71947008 | Homotransplant of pancreas |
719522009 | Infection of upper respiratory tract caused by Candida co-occurrent with human immunodeficiency virus infection |
719685004 | Absent thumb with short stature and immunodeficiency syndrome |
719789000 | Human immunodeficiency virus 2 antibody positive and Human immunodeficiency virus 1 antibody cross-reactivity |
719814009 | X-linked mendelian susceptibility to mycobacterial disease |
719824001 | Vici syndrome |
719827008 | X-linked immunoneurologic disorder |
720345008 | Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome |
720520009 | Attenuated Chédiak-Higashi syndrome |
720853005 | Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome |
720986005 | Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome |
721095007 | Diaphragmatic defect, limb deficiency, skull defect syndrome |
721166000 | Human immunodeficiency virus complicating pregnancy childbirth and the puerperium |
721303001 | Refractory neutropenia |
721305008 | Acute myeloid leukemia due to recurrent genetic abnormality |
721306009 | Therapy related acute myeloid leukemia and myelodysplastic syndrome |
721308005 | Acute leukemia of ambiguous lineage |
721310007 | Aggressive natural killer-cell leukemia |
721555001 | Follicular lymphoma of small intestine |
721762007 | Adult T-cell leukemia/lymphoma of skin |
721876004 | Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency |
721877008 | Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency |
721903007 | Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome |
721977007 | Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome |
722067005 | Severe combined immunodeficiency with hypereosinophilia |
722281001 | Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome |
722288007 | Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome |
722290008 | Autoimmune lymphoproliferative syndrome with recurrent viral infection |
722386009 | Celiac disease with epilepsy and cerebral calcification syndrome |
722401001 | Severe fever with thrombocytopenia syndrome virus |
722557007 | Parkinsonism due to human immunodeficiency virus infection |
72272002 | Non malignant mast cell disease |
722795004 | Meningeal leukemia |
722921008 | Neonatal hemorrhage of spleen |
722953004 | B-cell lymphoma unclassifiable with features intermediate between Burkitt lymphoma and diffuse large B-cell lymphoma |
722954005 | B-cell lymphoma unclassifiable with features intermediate between classical Hodgkin lymphoma and diffuse large B-cell lymphoma |
722955006 | Chronic lymphoproliferative disorder of natural killer cells |
723334006 | Immunodeficiency due to mutation of FAS-associated protein with death domain gene |
723384004 | Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency |
723385003 | Mendelian susceptibility to mycobacterial disease due to partial interferon regulatory factor 8 deficiency |
723386002 | Mendelian susceptibility to mycobacterial disease due to partial signal transducer and activator of transcription 1 deficiency |
723443003 | Neutrophil immunodeficiency syndrome |
723508002 | RAS-associated autoimmune leukoproliferative disease |
723512008 | Revesz syndrome |
723889003 | B lymphoblastic leukemia lymphoma with t(9:22) (q34;q11.2); BCR-ABL 1 |
723995003 | Schimke immuno-osseous dysplasia |
724015007 | Pyogenic arthritis, pyoderma gangrenosum, acne syndrome |
724177005 | Ligase 4 syndrome |
724179008 | Laron syndrome with immunodeficiency |
72425000 | Bilateral left-sidedness sequence |
724275005 | Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency |
724276006 | X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome |
724361001 | Hepatic veno-occlusive disease with immunodeficiency syndrome |
724638006 | Splenomegaly co-occurrent and due to storage disease |
724639003 | Asplenia following surgical procedure |
724641002 | Primary hemophagocytic lymphohistiocytosis |
724644005 | Myeloid leukemia co-occurrent with Down syndrome |
724645006 | T-cell histiocyte rich large B-cell lymphoma |
724647003 | Diffuse large B-cell lymphoma co-occurrent with chronic inflammation caused by Epstein-Barr virus |
724648008 | Plasmablastic lymphoma |
725135004 | Combined immunodeficiency due to CD3gamma deficiency |
725136003 | Immunodeficiency by defective expression of human leukocyte antigen class 1 |
725137007 | Neutropenia, monocytopenia, deafness syndrome |
725150008 | Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency |
725151007 | Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency |
725290000 | Combined immunodeficiency due to partial recombination-activating gene 1 deficiency |
725390002 | Acute myeloid leukemia with t(8;16)(p11;p13) translocation |
725431001 | Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency |
725432008 | Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency |
725437002 | Chronic lymphocytic leukemia genetic mutation variant |
726078000 | Sporadic Blau syndrome |
72621000119104 | Human immunodeficiency virus (HIV) II infection category B1 |
726708009 | Familial isolated congenital asplenia |
726721002 | Nodal marginal zone B-cell lymphoma |
733598001 | Acute myeloid leukemia with t(6;9)(p23;q34) translocation |
733627006 | Primary cutaneous gamma-delta-positive T-cell lymphoma |
733834006 | Invasive carcinoma of uterine cervix co-occurrent with human immunodeficiency virus infection |
733835007 | Extrapulmonary tuberculosis co-occurrent with human immunodeficiency virus infection |
734066005 | Diffuse large B-cell lymphoma of central nervous system |
734522002 | Acute myeloid leukemia with FMS-like tyrosine kinase-3 mutation |
735332000 | Primary cutaneous diffuse large cell B-cell lymphoma of lower extremity |
735521001 | Human immunodeficiency virus World Health Organization 2007 stage 1 co-occurrent with tuberculosis |
735522008 | Human immunodeficiency virus World Health Organization 2007 stage 1 co-occurrent with malaria |
735523003 | Human immunodeficiency virus World Health Organization 2007 stage 2 co-occurrent with tuberculosis |
735524009 | Human immunodeficiency virus World Health Organization 2007 stage 2 co-occurrent with malaria |
735525005 | Human immunodeficiency virus World Health Organization 2007 stage 3 co-occurrent with tuberculosis |
735526006 | Human immunodeficiency virus World Health Organization 2007 stage 3 co-occurrent with malaria |
735527002 | Human immunodeficiency virus World Health Organization 2007 stage 4 co-occurrent with tuberculosis |
735528007 | Human immunodeficiency virus World Health Organization 2007 stage 4 co-occurrent with malaria |
735536003 | Adult-onset immunodeficiency |
736322001 | Pediatric follicular lymphoma |
737307003 | Natural-killer cell deficiency |
737378009 | World Health Organization 2007 Human immunodeficiency virus infection clinical stage 1 |
737379001 | World Health Organization 2007 Human immunodeficiency virus infection clinical stage 2 |
737380003 | World Health Organization 2007 Human immunodeficiency virus infection clinical stage 3 |
737381004 | World Health Organization 2007 Human immunodeficiency virus infection clinical stage 4 |
738770003 | Anaplastic lymphoma kinase positive anaplastic large cell lymphoma |
739301006 | Osteoporosis co-occurrent and due to multiple myeloma |
76077004 | Total pancreatectomy with transplantation |
762315004 | Therapy related acute myeloid leukemia due to and following administration of antineoplastic agent |
762316003 | Polymorphic lymphoproliferative disorder following transplant |
76243000 | Chronic granulomatous disease, type IVA |
762690000 | Classical Hodgkin lymphoma |
763309005 | Acute myeloid leukemia with nucleophosmin 1 somatic mutation |
763477007 | Primary lymphoma of conjunctiva |
763623001 | Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency |
763666008 | Splenic marginal zone B-cell lymphoma |
763668009 | Lichtenstein syndrome |
763713000 | Idiopathic CD4 lymphocytopenia |
763719001 | Hydroa vacciniforme-like lymphoma |
763796007 | Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) |
763884007 | Splenic diffuse red pulp small B-cell lymphoma |
764855007 | Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation |
764858009 | Isolated agammaglobulinemia |
764940002 | Inherited acute myeloid leukemia |
764946008 | Constitutional mismatch repair deficiency syndrome |
765136002 | Primary cutaneous CD8 positive aggressive epidermotropic cytotoxic T-cell lymphoma |
765145001 | T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency |
765188009 | Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency |
765327005 | Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome |
765328000 | Classic mycosis fungoides |
766045006 | Acute myeloid leukemia and myelodysplastic syndrome related to alkylating agent |
766046007 | Acute myeloid leukemia and myelodysplastic syndrome related to topoisomerase type 2 inhibitor |
766048008 | Acute myeloid leukemia and myelodysplastic syndrome related to radiation |
766705006 | Immunodeficiency due to ficolin 3 deficiency |
766752000 | Neurolymphomatosis |
766879006 | Combined immunodeficiency due to OX40 deficiency |
766935007 | Primary bone lymphoma |
766983005 | Susceptibility to respiratory infection associated with CD8alpha chain mutation |
76762001 | Eosinophilic myopathy |
768556005 | Ataxia pancytopenia syndrome |
768560008 | Melanoma differentiation-associated gene 5 deficiency |
769167005 | Vaso-occlusive pain co-occurrent and due to sickle cell disease |
770593004 | Refractory celiac disease |
770625006 | Combined immunodeficiency with faciooculoskeletal anomalies syndrome |
770785002 | T-cell immunodeficiency due to ras homolog family member H deficiency |
77084001 | Immunologic aplastic anemia |
770942003 | Kostmann syndrome |
770947009 | Autosomal dominant severe congenital neutropenia |
771073006 | Lymphoproliferative disorder caused by methotrexate |
77121009 | X-linked lymphoproliferative syndrome |
771309000 | Autosomal recessive lymphoproliferative disease |
771333006 | Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection syndrome |
771443008 | Complement component 3 deficiency |
771471002 | Optic nerve edema, splenomegaly syndrome |
771479000 | Combined immunodeficiency due to serine/threonine kinase 4 deficiency |
771515001 | Facial dysmorphism, immunodeficiency, livedo, short stature syndrome |
771517009 | Severe combined immunodeficiency due to caspase recruitment domain family member 11 deficiency |
772126000 | Poikiloderma with neutropenia |
77330006 | Chronic granulomatous disease, type II |
773404000 | Roifman syndrome |
77358003 | Congenital leukocyte adherence deficiency |
773646003 | Phospholipase C gamma 2 associated antibody deficiency and immune dysregulation |
773662009 | Neonatal inflammatory skin and bowel disease |
773730002 | Osteopetrosis hypogammaglobulinemia syndrome |
773995001 | Primary cutaneous anaplastic large cell lymphoma |
774071007 | Pancytopenia with developmental delay syndrome |
775909002 | Congenital neutropenia, myelofibrosis, nephromegaly syndrome |
778004006 | Autoinflammation phospholipase C gamma 2 associated antibody deficiency and immune dysregulation |
778024005 | Monocytopenia with susceptibility to infections |
778028008 | Immunodeficiency due to CD25 deficiency |
778045003 | Susceptibility to viral and mycobacterial infection |
780817000 | Undifferentiated myeloproliferative disease |
780844005 | Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1 |
782750002 | T-cell receptor alpha-beta-positive T-cell deficiency |
782751003 | Severe combined immunodeficiency due to inhibitor of nuclear factor kappa B kinase subunit beta deficiency |
782759001 | X-linked dyserythropoietic anemia with abnormal platelets and neutropenia |
782915004 | Acquired hemophagocytic lymphohistiocytosis associated with malignant disease |
783007005 | Recurrent Neisseria infection due to factor D deficiency |
783058007 | Autosomal recessive severe congenital neutropenia due to glucose-6-phosphatase catalytic subunit 3 deficiency |
783099001 | Radiosensitivity, immunodeficiency, dysmorphic features, learning difficulties syndrome |
783142006 | Pancytopenia due to IKAROS family zinc finger 1 mutations |
783143001 | Noonan syndrome-like disorder with juvenile myelomonocytic leukemia |
783150002 | Iatrogenic immunodeficiency-associated lymphoproliferative disorder |
783199003 | Autosomal recessive severe congenital neutropenia due to jagunal homolog 1 deficiency |
783200000 | Autosomal recessive severe congenital neutropenia due to C-X-C motif chemokine receptor 2 deficiency |
783201001 | Autosomal recessive severe congenital neutropenia due to colony stimulating factor 3 receptor deficiency |
783205005 | Alopecia antibody deficiency |
783211008 | Non-chronic lymphocytic leukemia monoclonal B-cell lymphocytosis |
783245001 | Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection |
783248004 | Hyperimmunoglobulin M syndrome with susceptibility to opportunistic infection |
783254003 | Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome |
783255002 | Hereditary isolated aplastic anemia |
783541009 | Breast implant–associated anaplastic large-cell lymphoma |
783617001 | Severe combined immunodeficiency due to lymphocyte-specific protein-tyrosine kinase deficiency |
783621008 | Immunodeficiency with factor I anomaly |
783743009 | Combined immunodeficiency with granulomatosis |
78378009 | Isoimmune neutropenia |
784340000 | Combined immunodeficiency due to interleukin 21 receptor deficiency |
784392009 | Adult chronic idiopathic neutropenia |
784393004 | Adult-onset immunodeficiency with anti-interferon-gamma autoantibodies |
786855003 | Monoclonal B-cell lymphocytosis chronic lymphocytic leukemia-type |
79019005 | Human immunodeficiency virus II infection |
79268002 | Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes syndrome |
79336007 | Familial eosinophilia |
79369007 | Complication of transplanted pancreas |
7990002 | Immunoglobulinemia with isolated somatotropin deficiency |
80191000119101 | Symptomatic human immunodeficiency virus I infection |
80192004 | Massive parenchymal disruption of spleen with open wound into abdominal cavity |
80255009 | Maternal transfer neutropenia |
80369006 | Chronic neutrophilia |
80378000 | Neonatal hepatosplenomegaly |
81000119104 | Symptomatic human immunodeficiency virus infection |
81166004 | Properdin deficiency disease |
815011000000107 | Anaplastic lymphoma kinase positive anaplastic large cell lymphoma |
815361000000107 | Acute myeloid leukaemia with 11q23 abnormality |
82053000 | Splenic abscess |
820601000000103 | Refractory anaemia with multilineage dysplasia |
82286005 | Hyperimmunoglobulin M syndrome |
82317007 | Chronic granulomatous disease, type III |
82546001 | Reactive immunoproliferative disease |
82893001 | Splenic atrophy |
82966003 | Hereditary angioedema |
83270006 | Neoplastic pleural effusion |
847481000000109 | Follicular lymphoma grade 1 |
847631000000107 | Follicular lymphoma grade 2 |
847651000000100 | Follicular lymphoma grade 3 |
847691000000108 | Follicular lymphoma grade 3a |
847701000000108 | Follicular lymphoma grade 3b |
847741000000106 | Diffuse large B-cell lymphoma |
84828003 | Leukopenia |
85559002 | Pelger-Huët anomaly |
86006001 | Massive parenchymal disruption of spleen without open wound into abdominal cavity |
861371000000102 | Acquired absence of spleen |
863741000000108 | Clinical stage A chronic lymphocytic leukaemia |
863761000000109 | Clinical stage B chronic lymphocytic leukaemia |
863781000000100 | Clinical stage C chronic lymphocytic leukaemia |
86406008 | Human immunodeficiency virus infection |
866901000000103 | Eosinophilic bronchitis |
87117006 | Human immunodeficiency virus infection with acute lymphadenitis |
89454001 | Shwachman syndrome |
89655007 | Congenital neutropenia |
896561000000109 | Transplantation of stomach |
896581000000100 | Allotransplantation of stomach |
90681000119107 | Asymptomatic human immunodeficiency virus A1 infection |
90691000119105 | Asymptomatic human immunodeficiency virus A2 infection |
91637004 | Myasthenia gravis |
91854005 | Acute leukemia in remission |
91855006 | Acute leukemia, disease |
91856007 | Acute lymphoid leukemia in remission |
91857003 | Acute lymphoid leukemia, disease |
91858008 | Acute monocytic leukemia in remission |
91860005 | Acute myeloid leukemia in remission |
91861009 | Acute myeloid leukemia, disease |
91867008 | Adult form of celiac disease |
91923005 | Acquired immunodeficiency syndrome virus infection associated with pregnancy |
91947003 | Asymptomatic human immunodeficiency virus infection |
91948008 | Asymptomatic human immunodeficiency virus infection in pregnancy |
92508006 | Burkitt's tumor of intra-abdominal lymph nodes |
92509003 | Burkitt's tumor of intrapelvic lymph nodes |
92510008 | Burkitt's tumor of intrathoracic lymph nodes |
92511007 | Burkitt's tumor of lymph nodes of axilla AND/OR upper limb |
92512000 | Burkitt's tumor of lymph nodes of head, face AND/OR neck |
92513005 | Burkitt's tumor of lymph nodes of inguinal region AND/OR lower limb |
92514004 | Burkitt's tumor of lymph nodes of multiple sites |
92515003 | Burkitt's tumor of spleen |
92516002 | Burkitt's tumor of extranodal AND/OR solid organ site |
92754004 | Carcinoma in situ of spleen |
92811003 | Chronic leukemia in remission |
92812005 | Chronic leukemia, disease |
92813000 | Chronic lymphoid leukemia in remission |
92814006 | Chronic lymphoid leukemia, disease |
92817004 | Chronic myeloid leukemia in remission |
92818009 | Chronic myeloid leukemia, disease |
93030006 | Congenital absence of spleen |
93140007 | Letterer-Siwe disease of spleen |
93142004 | Leukemia in remission |
93143009 | Leukemia, disease |
93144003 | Leukemic reticuloendotheliosis of intra-abdominal lymph nodes |
93145002 | Leukemic reticuloendotheliosis of intrapelvic lymph nodes |
93146001 | Leukemic reticuloendotheliosis of intrathoracic lymph nodes |
93147005 | Leukemic reticuloendotheliosis of lymph nodes of axilla AND/OR upper limb |
93148000 | Leukemic reticuloendotheliosis of lymph nodes of head, face AND/OR neck |
93149008 | Leukemic reticuloendotheliosis of lymph nodes of inguinal region AND/OR lower limb |
93150008 | Leukemic reticuloendotheliosis of lymph nodes of multiple sites |
93151007 | Hairy cell leukemia of spleen |
93152000 | Leukemic reticuloendotheliosis of extranodal AND/OR solid organ site |
93169003 | Lymphoid leukemia in remission |
93189002 | Malignant histiocytosis of spleen |
93191005 | Malignant lymphoma of intra-abdominal lymph nodes |
93192003 | Malignant lymphoma of intrapelvic lymph nodes |
93193008 | Malignant lymphoma of intrathoracic lymph nodes |
93194002 | Malignant lymphoma of lymph nodes of axilla AND/OR upper limb |
93195001 | Malignant lymphoma of lymph nodes of head, face AND/OR neck |
93196000 | Malignant lymphoma of lymph nodes of inguinal region AND/OR lower limb |
93197009 | Malignant lymphoma of lymph nodes of multiple sites |
93198004 | Malignant lymphoma of spleen |
93199007 | Malignant lymphoma of extranodal AND/OR solid organ site |
93292008 | Congenital hypoplasia of spleen |
93450001 | Erythroleukemia in remission |
93451002 | Erythroleukemia, FAB M6 |
93487009 | Hodgkin's disease, lymphocytic depletion of lymph nodes of axilla AND/OR upper limb |
93488004 | Hodgkin's disease, lymphocytic depletion of lymph nodes of head, face AND/OR neck |
93489007 | Hodgkin's disease, lymphocytic depletion of lymph nodes of inguinal region AND/OR lower limb |
93492006 | Hodgkin's disease, lymphocytic depletion of extranodal AND/OR solid organ site |
93493001 | Hodgkin's disease, lymphocytic-histiocytic predominance of intra-abdominal lymph nodes |
93494007 | Hodgkin's disease, lymphocytic-histiocytic predominance of intrapelvic lymph nodes |
93495008 | Hodgkin's disease, lymphocytic-histiocytic predominance of intrathoracic lymph nodes |
93496009 | Hodgkin's disease, lymphocytic-histiocytic predominance of lymph nodes of axilla AND/OR upper limb |
93497000 | Hodgkin's disease, lymphocytic-histiocytic predominance of lymph nodes of head, face AND/OR neck |
93498005 | Hodgkin's disease, lymphocytic-histiocytic predominance of lymph nodes of inguinal region AND/OR lower limb |
93500006 | Hodgkin's disease, lymphocytic-histiocytic predominance of spleen |
93501005 | Hodgkin's disease, lymphocytic-histiocytic predominance of extranodal AND/OR solid organ site |
93505001 | Hodgkin's disease, mixed cellularity of lymph nodes of axilla AND/OR upper limb |
93506000 | Hodgkin's disease, mixed cellularity of lymph nodes of head, face AND/OR neck |
93507009 | Hodgkin's disease, mixed cellularity of lymph nodes of inguinal region AND/OR lower limb |
93509007 | Hodgkin's disease, mixed cellularity of spleen |
93510002 | Hodgkin's disease, mixed cellularity of extranodal AND/OR solid organ site |
93514006 | Hodgkin's disease, nodular sclerosis of lymph nodes of axilla AND/OR upper limb |
93515007 | Hodgkin's disease, nodular sclerosis of lymph nodes of head, face AND/OR neck |
93516008 | Hodgkin's disease, nodular sclerosis of lymph nodes of inguinal region AND/OR lower limb |
93518009 | Hodgkin's disease, nodular sclerosis of spleen |
93519001 | Hodgkin's disease, nodular sclerosis of extranodal AND/OR solid organ site |
93520007 | Hodgkin's disease of intra-abdominal lymph nodes |
93521006 | Hodgkin's disease of intrapelvic lymph nodes |
93522004 | Hodgkin's disease of intrathoracic lymph nodes |
93523009 | Hodgkin's disease of lymph nodes of axilla AND/OR upper limb |
93524003 | Hodgkin's disease of lymph nodes of head, face AND/OR neck |
93525002 | Hodgkin's disease of lymph nodes of inguinal region AND/OR lower limb |
93526001 | Hodgkin's disease of lymph nodes of multiple sites |
93527005 | Hodgkin's disease of spleen |
93528000 | Hodgkin's disease of extranodal AND/OR solid organ site |
93530003 | Hodgkin's granuloma of intrapelvic lymph nodes |
93531004 | Hodgkin's granuloma of intrathoracic lymph nodes |
93532006 | Hodgkin's granuloma of lymph nodes of axilla AND/OR upper limb |
93533001 | Hodgkin's granuloma of lymph nodes of head, face AND/OR neck |
93534007 | Hodgkin's granuloma of lymph nodes of inguinal region AND/OR lower limb |
93536009 | Hodgkin's granuloma of spleen |
93537000 | Hodgkin's granuloma of extranodal AND/OR solid organ site |
93541001 | Hodgkin's paragranuloma of lymph nodes of axilla AND/OR upper limb |
93542008 | Hodgkin's paragranuloma of lymph nodes of head, face AND/OR neck |
93543003 | Hodgkin's paragranuloma of lymph nodes of inguinal region AND/OR lower limb |
93545005 | Hodgkin's paragranuloma of spleen |
93546006 | Hodgkin's paragranuloma of extranodal AND/OR solid organ site |
93547002 | Hodgkin's sarcoma of intra-abdominal lymph nodes |
93548007 | Hodgkin's sarcoma of intrapelvic lymph nodes |
93549004 | Hodgkin's sarcoma of intrathoracic lymph nodes |
93550004 | Hodgkin's sarcoma of lymph nodes of axilla AND/OR upper limb |
93551000 | Hodgkin's sarcoma of lymph nodes of head, face AND/OR neck |
93552007 | Hodgkin's sarcoma of lymph nodes of inguinal region AND/OR lower limb |
93554008 | Hodgkin's sarcoma of spleen |
93555009 | Hodgkin's sarcoma of extranodal AND/OR solid organ site |
94071006 | Primary malignant neoplasm of spleen |
94148006 | Megakaryocytic leukemia in remission |
943041000000105 | Human immunodeficiency virus disease resulting in haematological and immunological abnormalities |
94603006 | Secondary malignant neoplasm of spleen |
94686001 | Mixed cell type lymphosarcoma of intra-abdominal lymph nodes |
94687005 | Mixed cell type lymphosarcoma of intrapelvic lymph nodes |
94688000 | Mixed cell type lymphosarcoma of intrathoracic lymph nodes |
94690004 | Mixed cell type lymphosarcoma of lymph nodes of head, face, and neck |
94704006 | Multiple myeloma in remission |
94707004 | Mycosis fungoides of intra-abdominal lymph nodes |
94708009 | Mycosis fungoides of intrapelvic lymph nodes |
94709001 | Mycosis fungoides of intrathoracic lymph nodes |
94710006 | Mycosis fungoides of lymph nodes of axilla AND/OR upper limb |
94711005 | Mycosis fungoides of lymph nodes of head, face AND/OR neck |
94712003 | Mycosis fungoides of lymph nodes of inguinal region AND/OR lower limb |
94714002 | Mycosis fungoides of spleen |
94715001 | Mycosis fungoides of extranodal AND/OR solid organ site |
94716000 | Myeloid leukemia in remission |
94718004 | Myeloid sarcoma in remission |
94719007 | Myeloid sarcoma, disease |
95111006 | Neoplasm of uncertain behavior of spleen |
95186006 | Nodular lymphoma of intra-abdominal lymph nodes |
95187002 | Nodular lymphoma of intrapelvic lymph nodes |
95188007 | Nodular lymphoma of intrathoracic lymph nodes |
95192000 | Nodular lymphoma of lymph nodes of multiple sites |
95193005 | Nodular lymphoma of spleen |
95194004 | Nodular lymphoma of extranodal AND/OR solid organ site |
95209008 | Plasma cell leukemia in remission |
95210003 | Plasma cell leukemia, disease |
95224004 | Reticulosarcoma of intra-abdominal lymph nodes |
95225003 | Reticulosarcoma of intrapelvic lymph nodes |
95226002 | Reticulosarcoma of intrathoracic lymph nodes |
95230004 | Reticulosarcoma of lymph nodes of multiple sites |
95231000 | Reticulosarcoma of spleen |
95260009 | Sézary's disease of lymph nodes of head, face AND/OR neck |
95261008 | Sézary's disease of lymph nodes of inguinal region AND/OR lower limb |
95263006 | Sézary's disease of spleen |
95264000 | Sézary's disease of extranodal AND/OR solid organ site |
95416007 | Eosinophilia myalgia syndrome |
95624007 | Neonatal lymphocytopenia |
95733001 | Eosinophilic keratitis |
95846001 | Red blood cell sequestration in spleen |
95892003 | Persistent generalized lymphadenopathy |
9893005 | Immunodeficiency with thymoma |
Codes not in the full codelist are in faint grey.