Phenotype #0000207651

Individual ID 00269858
Associated disease CAKUT
Phenotype details non-neurogenic, neurogenic bladder, left hydronephrosis, right cystic kidney, hypospadias, impaired pupillary light reflex, flat cardiotocography tracing in utero
Diagnosis/Initial CAKUT
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-12-07 18:05:38 +01:00 (CET)
Date last edited 2019-12-07 18:15:02 +01:00 (CET)

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