Amyloidosis, hereditary systemic 3

Preferred Label : Amyloidosis, hereditary systemic 3;

Symbol : AMYLD3;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Amyloidosis, type iv; Amyloidosis, iowa type; Amyloidosis, van allen type; Amyloidosis, type III;

Prefixed ID : #620657;

Détails

Origin ID

620657;

UMLS CUI

C4551500;

Genes related to phenotype
- Apolipoprotein a-I [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial amyloid polyneuropathy, Iowa type (disorder) [SNOMED CT concept]

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