Hereditary renal agenesis

A group of perinatally lethal renal diseases that include bilateral renal aplasia, unilateral renal agenesis with contralateral dysplasia (URA/RD), and severe obstructive uropathy. Germline mutations in the ITGA8 and RET genes have been identified (OMIM: 191830). Renal aplasia is the most severe congenital anomaly of the kidney and urinary tract and is caused by a heterozygous DSTYK mutation (OMIM: 610805).

Also Known As:

Bilateral renal agenesis; Potter Syndrome; Renal agenesis; Urogenital adysplasia, hereditary

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Hereditary renal agenesis: 166
Urogenital System
- Urinary Tract
  - Kidney
    - Hereditary renal agenesis: 166
Urogenital Diseases: 126
- Urologic Diseases: 799
  - Kidney Diseases: 12250
    - Hereditary renal agenesis: 166
- Female Urogenital Diseases and Pregnancy Complications
  - Female Urogenital Diseases
    - Urologic Diseases: 799
      - Kidney Diseases: 12250
        Hereditary renal agenesis: 166
- Male Urogenital Diseases
  - Urologic Diseases: 799
    - Kidney Diseases: 12250
      - Hereditary renal agenesis: 166

Pinaki R Debnath Selected Research

Pinaki R Debnath Research Topics

Disease

Drug/Important Bio-Agent (IBA)