OBO ID: DOID:0080874
Term Name: primary ovarian insufficiency 17 Search Ontology:
Synonyms:
Definition: A primary ovarian insufficiency that is characterized by early cessation of menses after initial menarche, with small ovaries and uterus and that has_material_basis_in homozygous mutation in the XRCC2 gene on chromosome 7q36. https://pubmed.ncbi.nlm.nih.gov/30489636/
References:
Ontology: Human Disease   ( DOID:0080874 )
Relationships
is a type of:
OTHER primary ovarian insufficiency 17 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
XRCC2 ?Premature ovarian failure 17 619146
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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