Phenotype #0000350777

Individual ID 00465242
Associated disease renal failure
Phenotype details HP:0000089, HP:0000104, HP.0008678, HP:0010958, HP:0012584, HP:0012582, HP:0001627, HP:0001638, HP:0011723, HP:0045017, HP:0002089
Diagnosis/Initial multiple congenital abnormalities, renal agenesis
Inheritance Familial, autosomal dominant
Diagnosis/Definite RHDA3
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Marketa Wayhelova
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Marketa Wayhelova
Date created 2025-04-26 11:47:24 +02:00 (CEST)
Date last edited 2025-05-01 15:57:10 +02:00 (CEST)

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