Disease #04607 (CAKUTHED (anomalies, congenital, kidney and urinary tract syndrome with/without hearing loss, abnormal ears, or developmental delay (CAKUTHED)), OMIM:176310)

Official abbreviation CAKUTHED
Name anomalies, congenital, kidney and urinary tract syndrome with/without hearing loss, abnormal ears, or developmental delay (CAKUTHED)
OMIM ID 176310
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PBX1
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2019-01-21 13:18:35 +01:00 (CET)

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