Phenotype #0000303453

Individual ID 00411413
Associated disease HP1
Phenotype details stone disease with nephrocalcinosis
Diagnosis/Initial oxalosis
Inheritance Familial, autosomal recessive
Diagnosis/Definite Primary hyperoxaluria
Age/Examination 08y (8 years)
Age/Diagnosis 08y
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 11:44:46 +02:00 (CEST)
Date last edited 2022-06-17 10:57:08 +02:00 (CEST)

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