Global Variome shared LOVD

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Phenotype #0000106134 Individual ID 00133387 Associated disease LGMDR5;LGMD2C Phenotype details clinical grade III; >31y-inable to walk (HP:0002540) Diagnosis/Initial severe autosomal recessive muscular dystrophy, North African type (SCARMD) Inheritance Familial Diagnosis/Definite - Age/Examination - Age/Diagnosis 15y Age/Onset - Phenotype/Onset exercise intolerance Protein IHC SGC weak, SSPN weak Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2007-07-02 13:52:56 +02:00 (CEST) Date last edited 2012-03-04 15:57:55 +01:00 (CET)

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