Global Variome shared LOVD

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

Phenotype #0000105516 Individual ID 00132746 Associated disease NICCD Phenotype details hyperammonemia, hypercitrullinemia, galactosemia Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination <00y01m (before 1 month) Age/Diagnosis 00y05m Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2017-11-03 17:49:11 +01:00 (CET) Date last edited 2017-11-03 17:52:13 +01:00 (CET)

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