Global Variome shared LOVD

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

Phenotype #0000119330 Individual ID 00146641 Associated disease LGMD2 Phenotype details hyperCKemia (CPK 22x), able to walk Diagnosis/Initial dystrophy, muscular, limb-girdle, autosomal recessive Diagnosis/Definite - Inheritance Isolated (sporadic) Age/Examination - Age/Onset 26y Phenotype/Onset - Age/Diagnosis - Protein IHC: DAG1 absent Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2007-08-31 17:44:39 +02:00 (CEST) Date last edited 2012-03-09 19:02:28 +01:00 (CET)

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