Global Variome shared LOVD

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

Phenotype #0000303405 Individual ID 00411366 Associated disease HP1 Phenotype details - Diagnosis/Initial oxalosis Inheritance Familial, autosomal recessive Diagnosis/Definite Primary hyperoxaluria Age/Examination 08y (8 years) Age/Diagnosis 08y 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 10:02:22 +02:00 (CEST) Date last edited 2022-06-17 10:51:21 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.