Hypoalphalipoproteinemia, primary, 2, intermediate

Preferred Label : Hypoalphalipoproteinemia, primary, 2, intermediate;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Hypoalphalipoproteinemia, primary, 2, autosomal dominant;

Prefixed ID : #619836;

Détails

Origin ID

619836;

UMLS CUI

C5677030;

Genes related to phenotype
- Apolipoprotein a-I [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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