ZFIN Human Disease: ovarian dysgenesis 6

OBO ID: DOID:0080498

Term Name:	ovarian dysgenesis 6		Search Ontology:
Synonyms:
Definition:	A 46 XX gonadal dysgenesis that has_material_basis_in homozygous mutation in the NUP107 gene on chromosome 12q15. https://www.omim.org/entry/618078
References:	OMIM:618078
Ontology:	Human Disease ( DOID:0080498 )

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 6 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NUP107	nup107	?Ovarian dysgenesis 6	618078

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None