ZFIN Human Disease: primary ovarian insufficiency 7

OBO ID: DOID:0080864

Term Name:	primary ovarian insufficiency 7		Search Ontology:
Synonyms:
Definition:	A primary ovarian insufficiency that has_material_basis_in heterozygous mutation in the NR5A1 gene on chromosome 9q33. https://pubmed.ncbi.nlm.nih.gov/26523528/
References:	OMIM:612964
Ontology:	Human Disease ( DOID:0080864 )

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 7 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NR5A1	nr5a1b nr5a1a	Adrenocortical insufficiency	612964
		Premature ovarian failure 7	612964

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None