Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

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 International 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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