Asplenia and splenic dysfunction codes
Codelist metadata
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Coding system
- SNOMED CT
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Coding system release
- unknown
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Organisation
- NHSD Primary Care Domain Refsets
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Codelist ID
- nhsd-primary-care-domain-refsets/splenic_cod
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Version Tag
- 20211221
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Version ID
- 022f0220
Versions
About
Description
Taken from the SPLENIC_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 |
---|---|
1003551006 | Agenesis of spleen |
143551000119106 | Chronic thrombosis of splenic vein |
14534009 | Splenic vein thrombosis |
155842007 | Coeliac disease |
161626009 | History of splenectomy |
174776001 | Total splenectomy |
17604001 | Bilateral right-sidedness sequence |
186792002 | Plasmodium vivax malaria with rupture of spleen |
197478000 | Congenital celiac disease |
197479008 | Acquired celiac disease |
197481005 | Celiac disease NOS |
205735005 | Hypoplasia of spleen |
22996003 | Splenic infarction |
234319005 | Splenectomy |
234513007 | Post-splenectomy leukocytosis |
23761004 | Hyposplenism |
23829007 | Celiac disease |
25167006 | Perisplenitis |
262821002 | Avulsion of spleen |
266478000 | Coeliac disease |
275404008 | Celiac rickets |
300564004 | Spleen absent |
302961007 | Hereditary splenic hypoplasia |
314118002 | Laparoscopic total splenectomy |
38096003 | Functional asplenia |
396330006 | Celiac crisis |
396331005 | Celiac disease |
444108000 | Acute sickle cell splenic sequestration crisis |
45259000 | Celiac infantilism |
56338005 | Splenic fibrosis |
606731000000100 | Celiac disease NOS |
61715008 | Celiac disease with diffuse intestinal ulceration |
702624008 | Aplasia of spleen |
707147002 | Asplenia |
711407000 | Thrombocytopathy, asplenia and miosis |
722386009 | Celiac disease with epilepsy and cerebral calcification syndrome |
722921008 | Neonatal hemorrhage of spleen |
724639003 | Asplenia following surgical procedure |
726708009 | Familial isolated congenital asplenia |
770593004 | Refractory celiac disease |
80192004 | Massive parenchymal disruption of spleen with open wound into abdominal cavity |
82893001 | Splenic atrophy |
86006001 | Massive parenchymal disruption of spleen without open wound into abdominal cavity |
861371000000102 | Acquired absence of spleen |
91867008 | Adult form of celiac disease |
93030006 | Congenital absence of spleen |
93140007 | Letterer-Siwe disease of spleen |
93292008 | Congenital hypoplasia of spleen |
Codes not in the full codelist are in faint grey.