Denys-Drash Syndrome D030321

Related MeSH Hierarchy (16)

Diseases [C] » Neoplasms [C04] » Neoplasms by Histologic Type » Neoplasms, Complex and Mixed » Wilms Tumor » Denys-Drash Syndrome

Diseases [C] » Urogenital Diseases [C12] » Male Urogenital Diseases » Urologic Diseases » Kidney Diseases » Kidney Neoplasms » Wilms Tumor » Denys-Drash Syndrome

Diseases [C] » Urogenital Diseases [C12] » Urogenital Neoplasms » Urologic Neoplasms » Kidney Neoplasms » Wilms Tumor » Denys-Drash Syndrome

Diseases [C] » Urogenital Diseases [C12] » Urologic Diseases » Kidney Diseases » Kidney Neoplasms » Wilms Tumor » Denys-Drash Syndrome

Diseases [C] » Urogenital Diseases [C12] » Urologic Diseases » Urologic Neoplasms » Kidney Neoplasms » Wilms Tumor » Denys-Drash Syndrome

Diseases [C] » Neoplasms [C04] » Neoplasms by Site » Urogenital Neoplasms » Urologic Neoplasms » Kidney Neoplasms » Wilms Tumor » Denys-Drash Syndrome

Diseases [C] » Neoplasms [C04] » Neoplastic Syndromes, Hereditary » Wilms Tumor » Denys-Drash Syndrome

Description

A disorder of sex development characterized by UROGENITAL ABNORMALITIES; GONADAL DYSGENESIS; and WILMS TUMOR. It is caused by a mutation in the Wilms tumor suppressor gene (GENES, WILMS TUMOR) on chromosome 11.   MeSH

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