Phenotype #0000304010

Individual ID 00411994
Associated disease HP2
Phenotype details -
Diagnosis/Initial oxalosis
Inheritance Familial, autosomal recessive
Diagnosis/Definite Primary hyperoxaluria
Age/Examination -
Age/Diagnosis -
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 2022-06-21 10:50:50 +02:00 (CEST)
Date last edited 2025-03-13 09:44:26 +01:00 (CET)

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