Global Variome shared LOVD

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

Phenotype #0000303533 Individual ID 00411496 Associated disease HP1 Phenotype details - Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite Primary hyperoxaluria Age/Examination 16y (16 years) Age/Diagnosis 16y 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 2022-06-14 11:48:10 +02:00 (CEST) Date last edited 2022-06-17 10:43:23 +02:00 (CEST)

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