OBO ID: DOID:0080858
Term Name: primary ovarian insufficiency 2A Search Ontology:
Synonyms:
Definition: A primary ovarian insufficiency that has_material_basis_in mutation in the DIAPH2 gene on chromosome Xq22. https://pubmed.ncbi.nlm.nih.gov/9497258/
References:
Ontology: Human Disease   ( DOID:0080858 )
Relationships
is a type of:
OTHER primary ovarian insufficiency 2A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DIAPH2 ?Premature ovarian failure 2A 300511
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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