OMOP Concept 37109308
Hereditary amyloidosis
StandardConditionSNOMED367601000119103Disorder
Maps from
4
Descendants
31
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
4 source codes normalize to Hereditary amyloidosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 125088 | Systemic amyloidosis | Non-standard |
| CIEL | 138796 | Hereditary Cerebrovascular Amyloidosis | Non-standard |
| CIEL | 155078 | Amyloidogenic transthyretin amyloidosis | Non-standard |
| MeSH | D028226 | Amyloidosis, Familial | Non-standard |
Synonyms
Alternative names recorded for Hereditary amyloidosis across source vocabularies.
- amiloidosis hereditaria
- amiloidosis hereditaria (trastorno)
- Hereditary amyloidosis (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(5)Roll up to these when you need a wider cohort.
Narrower concepts
(31)Included automatically when you query with descendants.
- 1AGel amyloidosis
- 1Autosomal dominant beta2-microglobulinic amyloidosis
- 1Familial amyloid nephropathy with urticaria AND deafness
- 1Familial amyloid polyneuropathy
- 1Gelatinous droplike corneal dystrophy
- 1Hereditary ATTR amyloidosis
- 1Hereditary cerebrovascular amyloidosis
- 1Hereditary oculoleptomeningeal amyloid angiopathy
- 1Hereditary systemic amyloidosis
- 1Heredofamilial systemic amyloidosis affecting skin
- 1ITM2B-related amyloidosis
- 1Localized hereditary amyloidosis
- 1Prion protein systemic amyloidosis
- 2ABri amyloidosis
- 2ADan amyloidosis
- 2Amyloid polyneuropathy type I
- 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
- 2Familial lichen amyloidosis
- 2Hereditary cerebral hemorrhage with amyloidosis
- 2Lattice corneal dystrophy
- 2Localized hereditary cardiac amyloidosis
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