ZFIN Human Disease: primary ovarian insufficiency 13

OBO ID: DOID:0080870

Term Name:	primary ovarian insufficiency 13		Search Ontology:
Synonyms:
Definition:	A primary ovarian insufficiency that has_material_basis_in homozygous mutation in the MSH5 gene on chromosome 6p21. https://pubmed.ncbi.nlm.nih.gov/28175301/
References:	OMIM:617442
Ontology:	Human Disease ( DOID:0080870 )

Relationships

is a type of:	autosomal recessive disease primary ovarian insufficiency autosomal recessive disease primary ovarian insufficiency Show first 5 Terms

OTHER primary ovarian insufficiency 13 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MSH5	msh5	?Premature ovarian failure 13	617442

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None