Global Variome shared LOVD

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Phenotype #0000119309 Individual ID 00146570 Associated disease LGMD2 Phenotype details see paper; ... Diagnosis/Initial dystrophy, muscular, limb-girdle, autosomal recessive Diagnosis/Definite MDDGC5;LGMD2I Inheritance Familial, autosomal recessive Age/Examination 127 Age/Onset - Phenotype/Onset - Age/Diagnosis - Protein - Owner name Rolf Stucka Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2007-08-31 17:40:57 +02:00 (CEST) Date last edited 2026-07-03 19:58:56 +02:00 (CEST)

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