46,XX sex reversal 5

Summary
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.
Super Class
46,XX sex reversal autosomal dominant disease
External Links
Disease Ontology
DOID:0080943
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7026 NR2F2 nuclear receptor subfamily 2 group F member 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
11819 Nr2f2 nuclear receptor subfamily 2, group F, member 2

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024