Phenotype #0000163886

Individual ID 00215434
Associated disease LGMD
Phenotype details lost ability to walk (HP:0006957)
Diagnosis/Initial limb-girdle muscular dystrophy
Inheritance Isolated (sporadic)
Diagnosis/Definite LGMD2B
Age/Examination -
Age/Diagnosis >68y
Age/Onset 40y
Phenotype/Onset -
Protein IHC DYSF severly reduced
Owner name Nicolas Levy
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2007-12-28 14:43:34 +01:00 (CET)
Date last edited 2020-10-04 11:04:50 +02:00 (CEST)

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