Myopia 25, autosomal dominant

Preferred Label : Myopia 25, autosomal dominant;

Symbol : MYP25;

CISMeF acronym : MYP25;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the procollagen-proline, 2-oxoglutarate-4-dioxygenase, alpha-subunit, isoform-2 gene (P4HA2, 600608.0001);

Prefixed ID : #617238;

Details

Origin ID

617238;

UMLS CUI

C4310655;

Genes related to phenotype
- Procollagen-proline, 2-oxoglutarate-4-dioxygenase, alpha subunit, isoform 2 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- High myopia [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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