Phenotype #0000236415

Individual ID 00311160
Associated disease CAKUT
Phenotype details upper urinary tract renal agenesis (L), lower urinary tract duplex urethra; club hand, hemi-vertebrae, vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities
Diagnosis/Initial CAKUT
Inheritance Isolated (sporadic)
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 2020-09-19 20:49:28 +02:00 (CEST)
Date last edited N/A

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