Global Variome shared LOVD

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

Phenotype #0000119568 Individual ID 00146997 Associated disease LGMD2 Phenotype details proximal muscle weakness. Diagnosis/Initial dystrophy, muscular, limb-girdle, autosomal recessive Diagnosis/Definite LGMD-2I Inheritance Familial, autosomal recessive Age/Examination - Age/Onset - Phenotype/Onset - Age/Diagnosis - Protein elevated CpK Owner name Tom Winder Database submission license No license selected Created by Tom Winder Date created 2012-10-19 18:08:18 +02:00 (CEST) Date last edited 2012-10-23 21:51:29 +02:00 (CEST)

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