Phenotype #0000352022

Individual ID 00466658
Associated disease PKD4
Phenotype details Multiple congenital anomalies, bilateral palpable kidney masses, dysmorphic features.
Diagnosis/Initial ARPKD
Inheritance Familial, autosomal recessive
Diagnosis/Definite ARPKD
Age/Examination 00y00m ()
Age/Diagnosis 00y00m
Age/Onset 00y00m
Phenotype/Onset -
Protein -
Owner name John Sayer
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by John Sayer
Date created 2025-09-18 22:22:09 +02:00 (CEST)
Date last edited 2025-10-02 12:30:18 +02:00 (CEST)

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