ZFIN Human Disease: primary ovarian insufficiency 10

OBO ID: DOID:0080867

Term Name:	primary ovarian insufficiency 10		Search Ontology:
Synonyms:
Definition:	A primary ovarian insufficiency that is characterized by primary amenorrhea, hypergonadotropic ovarian insufficiency, and genomic instability in somatic cells and that has_material_basis_in homozygous mutation in the MCM8 gene on chromosome 20p. https://pubmed.ncbi.nlm.nih.gov/25873734/
References:	OMIM:612885
Ontology:	Human Disease ( DOID:0080867 )

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 10 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MCM8	mcm8	?Premature ovarian failure 10	612885

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None