ZFIN Human Disease: primary ovarian insufficiency 3

OBO ID: DOID:0080860

Term Name:	primary ovarian insufficiency 3		Search Ontology:
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:	OMIM:608996
Ontology:	Human Disease ( DOID:0080860 )

Relationships

is a type of:	autosomal dominant disease primary ovarian insufficiency autosomal dominant disease primary ovarian insufficiency Show first 5 Terms

OTHER primary ovarian insufficiency 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
FOXL2	foxl2a foxl2b	Premature ovarian failure 3	608996

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None