ZFIN Human Disease: primary ovarian insufficiency 11

OBO ID: DOID:0080868

Term Name:	primary ovarian insufficiency 11		Search Ontology:
Synonyms:
Definition:	A primary ovarian insufficiency that is characterized by secondary amenorrhea and hypergonadotropic ovarian insufficiency, with elevated serum follicle-stimulating hormone levels before age 40 years and that has_material_basis_in heterozygous mutation in the ERCC6 gene on chromosome 10q11. https://pubmed.ncbi.nlm.nih.gov/26218421/
References:	OMIM:616946
Ontology:	Human Disease ( DOID:0080868 )

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 11 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ERCC6	ercc6	Premature ovarian failure 11	616946

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None