Global Variome shared LOVD

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

Phenotype #0000318943 Individual ID 00427997 Associated disease ? Diagnosis/Initial hypomagnesaemia Diagnosis/Definite HOMG1 Phenotype details hypomagnesaemia, seizures, developmental delay Inheritance Familial, autosomal recessive Age/Examination 01y (1 year) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2022-12-19 13:11:26 +01:00 (CET) Date last edited 2022-12-19 14:24:56 +01:00 (CET)

Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.