Lipodystrophy, familial partial, type 8

Preferred Label : Lipodystrophy, familial partial, type 8;

Symbol : FPLD8;

Type : Phenotype, molecular basis known;

Prefixed ID : #620679;

Details

Origin ID

620679;

UMLS CUI

C5882744;

Genes related to phenotype
- Alpha-2a-adrenergic receptor [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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