Myopia 26, X-linked, female-limited

Preferred Label : Myopia 26, X-linked, female-limited;

Symbol : MYP26;

CISMeF acronym : MYP26;

Type : Phenotype, molecular basis known;

Inheritance : X-linked (female limited);

Molecular basis : Caused by mutation in the retinal arrestin-3 gene (ARR3, 301770.0001);

Prefixed ID : #301010;

Details

Origin ID

301010;

UMLS CUI

C4538795;

Genes related to phenotype
- Arrestin 3, retinal [OMIM gene]
HPO term(s)
- High myopia [HPO term]
- X-linked inheritance [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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