ZFIN Human Disease: ovarian dysgenesis 3

OBO ID: DOID:0080495

Term Name:	ovarian dysgenesis 3		Search Ontology:
Synonyms:
Definition:	A 46 XX gonadal dysgenesis that has_material_basis_in homozygous mutation in the PSMC3IP gene on chromosome 17q12-q21. https://www.omim.org/entry/614324
References:	OMIM:614324
Ontology:	Human Disease ( DOID:0080495 )

Relationships

is a type of:	46 XX gonadal dysgenesis autosomal recessive disease 46 XX gonadal dysgenesis autosomal recessive disease Show first 5 Terms

OTHER ovarian dysgenesis 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
PSMC3IP	psmc3ip	Ovarian dysgenesis 3	614324

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None