Amyloidosis codes

Codelist metadata

Coding system

SNOMED CT

Coding system release

39.2.0

Organisation

NHSD Primary Care Domain Refsets

Codelist ID

nhsd-primary-care-domain-refsets/amyloidosis-codes

Version Tag

20241205

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.