Phenotype #0000106308

Individual ID 00133561
Associated disease LGMD
Phenotype details cardiomyopathy; >37y-inable to walk (HP:0002540)
Diagnosis/Initial dystrophy, muscular, limb-girdle (LGMD)
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 15y
Phenotype/Onset -
Protein IHC severly reduced SGCs, WB 10% SGCA
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2007-07-02 14:03:24 +02:00 (CEST)
Date last edited 2012-03-09 19:02:29 +01:00 (CET)

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