Amyloidosis codes
Codelist metadata
-
Coding system
- SNOMED CT
-
Coding system release
- 39.2.0
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Organisation
- NHSD Primary Care Domain Refsets
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Codelist ID
- nhsd-primary-care-domain-refsets/amyloidosis-codes
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Version Tag
- 20241205
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Version ID
- 4db3aed9
Versions
About
Description
Taken from the AMYLOID_COD
refset published by NHSD.
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 |
---|---|
111032003 | Macular cutaneous amyloidosis |
111390002 | Dominant primary localized cutaneous amyloidosis |
111391003 | Other localized amyloid deposit |
111392005 | Localized amyloid deposit |
11426004 | Gingival amyloidosis |
1148862002 | Deficiency of factor X due to systemic amyloidosis |
1156789004 | Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein |
1187126002 | Integral membrane protein 2B related amyloidosis |
1187147003 | Familial non-neuropathic amyloidosis of heart |
1187149000 | Localized hereditary amyloidosis of heart |
1187538003 | Secondary systemic amyloid angiopathy of cerebrum |
1187539006 | Non-neuropathic heredofamilial amyloidosis angiopathy of cerebrum |
1187540008 | Secondary systemic amyloidosis of heart |
1187553006 | Disorder of glomerulus due to secondary systemic amyloidosis |
1187554000 | Disorder of glomerulus due to familial amyloid polyneuropathy |
1187555004 | Disorder of glomerulus due to organ-limited amyloidosis |
1187557007 | Disorder of glomerulus due to amyloidosis |
1192004 | Familial amyloid neuropathy, Finnish type |
1228881003 | Leukocyte chemotactic factor-2 amyloidosis |
1231149005 | AH amyloidosis |
1259488005 | Dementia due to cerebral amyloid angiopathy |
129592008 | Amyloid polyneuropathy |
129593003 | Entrapment syndrome due to amyloid |
15123008 | Familial amyloid nephropathy with urticaria AND deafness |
154769007 | Amyloidosis |
16573007 | Senile cardiac amyloidosis |
1671000 | Sago spleen |
17602002 | Amyloidosis |
190923000 | Sporadic primary amyloidosis |
190925007 | Secondary amyloidosis |
190927004 | Primary amyloidosis NEC |
190928009 | Localised non-hereditary amyloidosis |
190929001 | [X]Heredofamilial amyloidosis, unspecified |
190930006 | Other specified amyloidosis |
190931005 | Amyloidosis NOS |
191113004 | [X]Other amyloidosis |
191121005 | [X]Heredofamilial amyloidosis, unspecified |
192918007 | Autonomic neuropathy due to amyloidosis |
193187004 | Polyneuropathy due to amyloidosis |
193247000 | Amyloid myopathy |
195228000 | Cerebral amyloid angiopathy |
196135008 | Pulmonary amyloidosis |
197604006 | Nephrotic syndrome in amyloidosis |
201337008 | Amyloidosis of skin |
201725009 | Arthritis secondary to amyloidosis |
209962000 | Myeloma-associated amyloidosis |
230359004 | Secondary amyloid encephalopathy |
230724001 | Cerebral amyloid angiopathy |
230725000 | Sporadic cerebral amyloid angiopathy |
230726004 | Icelandic type amyloidosis |
23132008 | Amyloid light-chain amyloidosis |
231928002 | Amyloid of cornea |
232076001 | Amyloid of vitreous |
232459006 | Laryngeal amyloidosis |
234510005 | Amyloidosis of spleen |
237864008 | AL amyloidosis |
237865009 | Primary amyloidosis of light chain type |
237866005 | Amyloid polyneuropathy type I |
237867001 | Hereditary cerebrovascular amyloidosis |
237868006 | Familial non-neuropathic amyloidosis |
237869003 | Localized hereditary amyloidosis |
237870002 | Familial lichen amyloidosis |
237871003 | Papular cutaneous amyloid |
237872005 | Poikilodermal cutaneous amyloid |
237873000 | Primary familial amyloid myopathy |
237874006 | Primary sporadic amyloid myopathy |
237875007 | Localized non-hereditary amyloidosis |
237876008 | Arthritis secondary to amyloidosis |
237877004 | Wild type ATTR amyloidosis |
27097002 | Danish type familial amyloid cardiomyopathy |
274545008 | [EDTA] Amyloid associated with renal failure |
274945004 | Amyloid A amyloidosis |
278899001 | Amyloid of urinary bladder |
281034005 | Reactive systemic amyloidosis |
281882003 | AD type amyloidosis |
282354001 | Amyloid of prostate |
282355000 | Amyloid of testes |
282357008 | Amyloid of ureter |
282834007 | Cutaneous amyloidosis |
302871005 | Primary amyloidosis |
302887008 | Neuropathy in secondary amyloidosis |
311495006 | Amyloid disease of the urethra |
32599008 | Hemodialysis-associated amyloidosis |
35080000 | Amyloidosis, type I |
361199007 | Lattice corneal dystrophy |
367528006 | Amyloidosis due to familial Mediterranean fever |
367601000119103 | Hereditary amyloidosis |
38606009 | Bullous cutaneous amyloidosis |
39502009 | Isolated atrial amyloid |
397883002 | Swedish type amyloid polyneuropathy |
397906009 | Portuguese type amyloid polyneuropathy |
397960001 | Andrade type amyloid polyneuropathy |
398163002 | Japanese type amyloid polyneuropathy |
398229007 | Amyloid polyneuropathy type I |
398247001 | Jewish type amyloid polyneuropathy |
402452001 | Primary systemic (AL fibril type) amyloidosis |
402453006 | Amyloid light chain amyloidosis due to multiple myeloma |
402454000 | Primary systemic amyloidosis due to occult plasma cell dyscrasia |
402455004 | Macroglossia due to amyloidosis |
402456003 | Pseudoscleroderma due to amyloid light-chain amyloidosis |
402457007 | Secondary systemic amyloidosis affecting skin (AA fibril type) |
402458002 | Hemodialysis-associated secondary amyloidosis of skin |
402459005 | Heredofamilial systemic amyloidosis affecting skin |
402460000 | Familial amyloid polyneuropathy with cutaneous amyloidosis |
402461001 | Maculopapular amyloidosis |
402462008 | Nodular amyloidosis |
402463003 | Familial localized cutaneous amyloidosis |
402464009 | Secondary localized cutaneous amyloidosis |
402719006 | Systemic amyloidosis affecting skin |
402720000 | Amyloidosis limited to skin |
40933005 | Isolated corneal amyloidosis |
413011000000101 | [X]Heredofamilial amyloidosis, unspecified |
415061000000103 | [X]Heredofamilial amyloidosis, unspecified |
41590007 | Familial amyloid polyneuropathy, Jewish type |
417939004 | Amyloid corneal degeneration |
418946006 | Lattice corneal dystrophy Type III |
419051009 | Polymorphic amyloid degeneration of cornea |
419087002 | Lattice corneal dystrophy Type II |
419197009 | Lattice corneal dystrophy Type I |
419398009 | Meretoja syndrome |
419900000 | Gelatinous droplike corneal dystrophy |
42295001 | Familial amyloid polyneuropathy |
425879009 | Amyloid A nephropathy |
426598005 | Amyloid light-chain nephropathy |
430081000000106 | Amyloid associated with renal failure - European Dialysis and Transplant Association |
43532007 | Hereditary oculoleptomeningeal amyloid angiopathy |
442012008 | Amyloidogenic transthyretin amyloidosis |
444231000000105 | [X]Other amyloidosis |
4463009 | Familial amyloid polyneuropathy, type II |
45502001 | Cerebrovascular amyloidosis |
45639009 | Hereditary cerebral amyloid angiopathy, Icelandic type |
4645000 | Senile brain amyloidosis |
48713002 | Amyloid nephropathy |
510351000000103 | AL amyloidosis |
5134006 | Familial amyloid polyneuropathy, type VI |
56453003 | Hereditary cerebral amyloid angiopathy, Dutch type |
56871000 | Localized amyloidosis |
57174000 | Focal amyloid |
58629009 | Dilated cardiomyopathy due to amyloidosis |
59017008 | Conjunctival amyloidosis |
598371000000106 | Amyloidosis NOS |
60733007 | Hypothyroidism due to amyloidosis |
61985005 | Primary localized cutaneous amyloidosis |
620101000000101 | Primary amyloidosis NEC |
633241000000101 | Other specified amyloidosis |
66451004 | Familial visceral amyloidosis, Ostertag type |
69078007 | Age-related amyloidosis |
700323004 | Amyloid pterygium |
703220002 | Hereditary cystatin C amyloid angiopathy |
703313007 | Cerebral amyloid angiopathy associated with systemic amyloidosis |
707090004 | Spondyloarthropathy due to hemodialysis-associated amyloidosis |
71041007 | Lattice corneal dystrophy |
715655000 | Transthyretin related familial amyloid cardiomyopathy |
716704007 | Primary localized cutaneous nodular amyloidosis |
718105008 | Lichen amyloidosis |
721661009 | Amyloidosis of small intestine |
722292000 | Autosomal dominant beta2-microglobulinic amyloidosis |
722948009 | Glomerular disorder due to non-neuropathic heredofamilial amyloidosis |
724357007 | Hereditary cerebral hemorrhage with amyloidosis |
733422008 | Prion protein systemic amyloidosis |
733729003 | Primary localized cutaneous amyloidosis |
764849002 | Amyloidosis cutis dyschromia |
783160006 | Hereditary gelsolin amyloidosis |
783161005 | Familial dementia British type |
783258000 | Familial dementia Danish type |
790731321000119100 | Lattice dystrophy of substantia propria of cornea of bilateral eyes |
79754008 | Restrictive cardiomyopathy secondary to amyloidosis |
8231007 | Ocular amyloid deposit |
84137001 | AA amyloidosis |
841951000000103 | Senile cardiac amyloidosis |
847041000000109 | Amyloid cardiomyopathy |
847051000000107 | Amyloid cardiomyopathy |
847141000000105 | Amyloidosis of stomach |
847151000000108 | Amyloid of stomach |
854071000000105 | Amyloidosis of intestine |
854081000000107 | Amyloidosis of intestine |
854091000000109 | Amyloidosis of small intestine |
854101000000101 | Amyloidosis of small intestine |
854111000000104 | Amyloidosis of large intestine |
854121000000105 | Amyloidosis of large intestine |
855161000000103 | Beta-2 microglobulin amyloidosis |
855181000000107 | Bullous cutaneous amyloidosis |
855291000000104 | Familial amyloid polyneuropathy type III |
855381000000105 | Amyloid nephropathy of Ostertag |
856771000000104 | Amyloid of bladder |
856901000000109 | Senile systemic amyloidosis |
857191000000102 | Amyloid of prostate |
857201000000100 | Amyloid disease of the urethra |
857231000000106 | Amyloid of vitreous |
857271000000108 | Familial amyloid polyneuropathy type II |
857291000000107 | Amyloid polyneuropathy type I |
857321000000102 | Senile cardiac amyloidosis |
857331000000100 | Amyloid A amyloidosis |
858181000000100 | Cerebrovascular amyloidosis |
858580008 | Secondary systemic amyloidosis |
874711000000100 | Cerebrovascular amyloidosis |
89449005 | Systemic amyloidosis |
9133005 | Familial amyloid polyneuropathy, Iowa type |
922941000000100 | Cutaneous amyloidosis |
922951000000102 | Cutaneous amyloidosis |
938241000000107 | Conjunctival amyloidosis |
9551004 | Hepatic amyloidosis |
Codes not in the full codelist are in faint grey.