Oculopharyngeal muscular dystrophy 2

Preferred Label : Oculopharyngeal muscular dystrophy 2;

Symbol : OPMD2;

Type : Phenotype, molecular basis known;

Prefixed ID : #620460;

Details

Origin ID

620460;

UMLS CUI

C5830682;

Genes related to phenotype
- Heterogeneous nuclear ribonucleoprotein a2/b1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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