46,XX sex reversal 5

Summary

DOID:0080943 - 46,XX sex reversal 5

Disease Ontology Definition:A 46,XX sex reversal that is characterized by genital virilization in 46,XX individuals, associated with congenital heart disease and variable somatic anomalies including blepharophimosis-ptosis-epicanthus inversus syndrome and congenital diaphragmatic hernia and that has_material_basis_in heterozygous mutation in the NR2F2 gene on chromosome 15q26.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: nr2f2

MIM:

MIM:618901 - 46,XX SEX REVERSAL 5; SRXX5

MIM:618901 - 46,XX SEX REVERSAL 5; SRXX5

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): 46,XX sex reversal (is_a), autosomal dominant disease (is_a)