Global Variome shared LOVD

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Phenotype #0000119318 Individual ID 00146583 Associated disease LGMD2 Phenotype details CPK >2000 Diagnosis/Initial dystrophy, muscular, limb-girdle, autosomal recessive Diagnosis/Definite LGMD-2I Inheritance Isolated (sporadic) Age/Examination - Age/Onset 5y Phenotype/Onset weakness of thighs since 5y Age/Diagnosis - Protein no LAMA2 reduction Owner name Lab Müller-Reible 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 2012-03-09 18:26:59 +01:00 (CET)

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