OMOP Concept 4232491
Systemic amyloidosis
StandardConditionSNOMED89449005Disorder
Maps from
1
Descendants
24
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Systemic amyloidosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 125088 | Systemic amyloidosis | Non-standard |
Synonyms
Alternative names recorded for Systemic amyloidosis across source vocabularies.
- amiloidosis sistémica
- amiloidosis sistémica (trastorno)
- Systemic amyloidosis (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
Narrower concepts
(24)Included automatically when you query with descendants.
- 1AH amyloidosis
- 1ALECT2 amyloidosis
- 1Apolipoprotein A-IV amyloidosis
- 1Familial amyloid polyneuropathy
- 1Hereditary ATTR amyloidosis
- 1Prion protein systemic amyloidosis
- 1Secondary systemic amyloidosis
- 1Systemic amyloidosis affecting skin
- 1Wild type ATTR amyloidosis
- 2AA amyloidosis
- 2AGel amyloidosis
- 2Amyloid of familial Mediterranean fever
- 2Amyloid polyneuropathy type I
- 2Cardiac secondary systemic amyloidosis
- 2Cerebral secondary systemic amyloid angiopathy
- 2Familial amyloid polyneuropathy, Iowa type
- 2Familial amyloid polyneuropathy, Jewish type
- 2Familial amyloid polyneuropathy, type II
- 2Familial amyloid polyneuropathy, type VI
- 2Familial amyloid polyneuropathy with cutaneous amyloidosis
- 2Heredofamilial systemic amyloidosis affecting skin
- 2Secondary systemic amyloidosis affecting skin (AA fibril type)
- 2Transthyretin related familial amyloid cardiomyopathy
- 3AA amyloid nephropathy
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