Phenotype #0000106117

Individual ID 00133370
Associated disease LGMDR5;LGMD2C
Phenotype details severe; 22y-inable to walk (HP:0002540)/10y-inable to walk (HP:0002540)-
Diagnosis/Initial severe autosomal recessive muscular dystrophy, North African type (SCARMD)
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis 07y-09y
Age/Onset -
Phenotype/Onset -
Protein -
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 13:52:57 +02:00 (CEST)
Date last edited 2012-03-09 19:02:29 +01:00 (CET)

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