Global Variome shared LOVD

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

Phenotype #0000274618 Individual ID 00380765 Associated disease MCC1D Phenotype details DD; ID; hypotonia; failure to thrive; acidosis (Neurological) Diagnosis/Initial - Inheritance Familial Diagnosis/Definite 3-Methylcrotonyl-CoA carboxylase 2 deficiency Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2021-08-23 12:15:23 +02:00 (CEST) Date last edited N/A

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