Phenotype #0000303465

Individual ID 00411425
Associated disease HP1
Phenotype details stone disease, nephrocalcinosis
Diagnosis/Initial oxalosis
Inheritance Familial, autosomal recessive
Diagnosis/Definite Primary hyperoxaluria
Age/Examination 03y (3 years)
Age/Diagnosis 03y
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 13:41:47 +02:00 (CEST)
Date last edited 2022-06-17 10:38:24 +02:00 (CEST)

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