ZFIN Human Disease: primary ovarian insufficiency 5

OBO ID: DOID:0080862

Term Name:	primary ovarian insufficiency 5		Search Ontology:
Synonyms:
Definition:	A primary ovarian insufficiency that has_material_basis_in heterozygous mutation in the NOBOX gene on chromosome 7q35. https://pubmed.ncbi.nlm.nih.gov/17701902/
References:	OMIM:611548
Ontology:	Human Disease ( DOID:0080862 )

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 5 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NOBOX	nobox	Premature ovarian failure 5	611548

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None