Search Ontology:
Human Disease

primary ovarian insufficiency 3

Term ID
DOID:0080860
Synonyms
Definition
A primary ovarian insufficiency that has_material_basis_in heterozygous mutation in the FOXL2 gene on chromosome 3q22. https://pubmed.ncbi.nlm.nih.gov/12149404/
References
  • MIM:608996
Ontology
Human Disease   ( DOID:0080860 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
Citations