Disease #07170 (CAKUT (Congenital Anomalies of the Kidney and Urinary Tract accompanied by cryptorchidism), OMIM:603054)

Official abbreviation CAKUT
Name Congenital Anomalies of the Kidney and Urinary Tract accompanied by cryptorchidism
OMIM ID 603054
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene GREM1
Associated tissues kidney
Disease features Renal hypoplasia, dysplasia, hydronephrosis (ureteropelvic junction obstruction or ureterovesical junction obstruction), ureteric duplex, vesicoureteral reflux, and posterior urethral valves. Possibly with cryptorchidism.
Remarks CAKUT is highly genetically heterogeneous.
Date created 2025-08-04 15:32:31 +02:00 (CEST)
Date last edited N/A

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