Global Variome shared LOVD

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

Phenotype #0000351776 Individual ID 00466412 Associated disease LGMDR10;LGMD2J Phenotype details Waddling gait, Proximal muscle weakness in lower limbs, Elevated serum creatine kinase, Muscular dystrophy Diagnosis/Initial LGMD Inheritance Familial, autosomal recessive Diagnosis/Definite LGMDR10 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Camille Verebi Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Created by Camille Verebi Date created 2025-08-27 14:30:29 +02:00 (CEST) Date last edited 2026-02-06 10:21:15 +01:00 (CET)

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