Phenotype #0000303462

Individual ID 00411422
Associated disease HP1
Phenotype details familial stone disease, nephrocalcinosis
Diagnosis/Initial oxalosis
Inheritance Familial, autosomal recessive
Diagnosis/Definite Primary hyperoxaluria
Age/Examination 00y06m (6 months)
Age/Diagnosis 00y08m
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Aiysha Abid
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Aiysha Abid
Date created 2022-06-13 12:35:40 +02:00 (CEST)
Date last edited 2022-06-17 10:36:26 +02:00 (CEST)

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