Disease #04607

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 0
Phenotype entries for this disease 0
Associated with 1 gene PBX1
Associated tissues -
Disease features autosomal dominant
Remarks -