Phenotype #0000303457

Individual ID 00411416
Associated disease HP1
Phenotype details -
Diagnosis/Initial oxalosis
Inheritance Familial, autosomal recessive
Diagnosis/Definite Primary hyperoxaluria
Age/Examination 02y05m (2 years, 5 months)
Age/Diagnosis 02y05m
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 12:11:39 +02:00 (CEST)
Date last edited 2022-06-17 10:34:54 +02:00 (CEST)

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