Global Variome shared LOVD

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

Phenotype #0000119711 Individual ID 00146847 Associated disease LGMD Phenotype details proximal muscle weakness, calf hypertrophy Diagnosis/Initial dystrophy, muscular, limb-girdle Inheritance Unknown Diagnosis/Definite LGMD2I Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Tom Winder Database submission license No license selected Created by Tom Winder Date created 2009-11-03 23:28:15 +01:00 (CET) Date last edited 2020-10-04 11:04:50 +02:00 (CEST)

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