ZFIN Human Disease: primary ovarian insufficiency 16

OBO ID: DOID:0080873

Term Name:	primary ovarian insufficiency 16		Search Ontology:
Synonyms:
Definition:	A primary ovarian insufficiency that is characterized by onset of amenorrhea early in the fourth decade of life, accompanied by elevated follicle-stimulating hormone levels and low estradiol levels and that has_material_basis_in heterozygous mutation in the BNC1 gene on chromosome 15q25. https://pubmed.ncbi.nlm.nih.gov/30010909/
References:	OMIM:618723
Ontology:	Human Disease ( DOID:0080873 )

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 16 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
BNC1	bnc1	?Premature ovarian failure 16	618723

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None