ZFIN Human Disease: primary ovarian insufficiency 19

OBO ID: DOID:0112278

Term Name:	primary ovarian insufficiency 19		Search Ontology:
Synonyms:	POF19 POI19 premature ovarian failure 19
Definition:	A primary ovarian insufficiency characterized by irregular menses that cease in the third decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the HSF2BP gene on chromosome 21q22. https://pubmed.ncbi.nlm.nih.gov/32845237/
References:	OMIM:619245
Ontology:	Human Disease ( DOID:0112278 )

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 19 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
HSF2BP	hsf2bp	Premature ovarian failure 19	619245

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None