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Congenital Anomalies Of Kidney And Urinary Tract 1 (MONDO:0012561)

Open Trait in OLS

Any congenital anomaly of kidney and urinary tract in which the cause of the disease is a mutation in the DSTYK gene.

Overview

Category

urinary system disorder

Ontology ID

Internal:13608

Synonyms

CAKUT1

DSTYK congenital anomaly of kidney and urinary tract

congenital anomalies of kidney and urinary tract 1

congenital anomaly of kidney and urinary tract caused by mutation in DSTYK

renal hypodysplasia, nonsyndromic, 1

Mapped terms

DOID:0080206

GARD:0024873

MEDGEN:322763

MESH:C563661

OMIM:610805

UMLS:C1835826

Child terms

Unknown children.

PH4038 Congenital Kidney Disease

BHF Data Science Centre Phenotype

Disease or syndrome

Kidney Data Science Catalyst

Coding Systems:

Ontology terms:

congenital anomalies of kidney and urinary tract 1

Last updated 2026-02-10 Samira Bell, Amy Coombe, Ross Forsyth, …