Premature ovarian failure 15

Preferred Label : Premature ovarian failure 15;

Symbol : POF15;

CISMeF acronym : POF15;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal recessive;

Molecular basis : Caused by mutation in the FANCM gene (FANCM, 609644.0005);

Prefixed ID : #618096;

Details

Origin ID

618096;

UMLS CUI

C4748170;

Genes related to phenotype
- Fancm gene [OMIM gene]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Oligomenorrhea [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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