Disease #02984 (CAKUT1;RHDNS1 (kidney and urinary tract, anomalies, congenital, susceptibility to, type 1 (CAKUT-1, renal hypodysplasia, nonsyndromic, type 1 (RHDNS-1))), OMIM:610805)

Official abbreviation CAKUT1;RHDNS1
Name kidney and urinary tract, anomalies, congenital, susceptibility to, type 1 (CAKUT-1, renal hypodysplasia, nonsyndromic, type 1 (RHDNS-1))
OMIM ID 610805
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene DSTYK
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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