ZFIN Human Disease: ovarian dysgenesis 7

OBO ID: DOID:0080499

Term Name:	ovarian dysgenesis 7		Search Ontology:
Synonyms:
Definition:	A 46 XX gonadal dysgenesis that has_material_basis_in homozygous mutation in the MRPS22 gene on chromosome 3q23. https://www.omim.org/entry/618117
References:	OMIM:618117
Ontology:	Human Disease ( DOID:0080499 )

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 7 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MRPS22	mrps22	Ovarian dysgenesis 7	618117

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None