OBO ID: DOID:0080870
Term Name: primary ovarian insufficiency 13 Search Ontology:
Synonyms:
Definition: A primary ovarian insufficiency that has_material_basis_in homozygous mutation in the MSH5 gene on chromosome 6p21. https://pubmed.ncbi.nlm.nih.gov/28175301/
References:
Ontology: Human Disease   (DOID:0080870)
OTHER primary ovarian insufficiency 13 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MSH5 ?Premature ovarian failure 13 617442
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None