ZFIN Human Disease: primary ovarian insufficiency 6

OBO ID: DOID:0080863

OBO ID: DOID:0080863

Term Name:	primary ovarian insufficiency 6	Search Ontology:
Synonyms:
Definition:	A primary ovarian insufficiency that has_material_basis_in heterozygous or homozygous mutation in the FIGLA gene on chromosome 2p13. https://pubmed.ncbi.nlm.nih.gov/18499083/
References:	OMIM:612310
Ontology:	Human Disease ( DOID:0080863 )

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 6 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
FIGLA	figla	Premature ovarian failure 6	612310

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None