Phenotype #0000106556

Individual ID 00133807
Associated disease LGMD
Phenotype details proximal muscle weakness lower extremity; 12y-loss ambulation; no cardiac involvement
Diagnosis/Initial dystrophy, muscular, limb-girdle (LGMD)
Inheritance Familial, autosomal recessive
Diagnosis/Definite LGMD2C
Age/Examination -
Age/Diagnosis -
Age/Onset 08y
Phenotype/Onset -
Protein -
Owner name Ieke Ginjaar
Database submission license No license selected
Created by Ieke Ginjaar
Date created 2007-07-13 16:38:45 +02:00 (CEST)
Date last edited 2020-10-04 12:59:14 +02:00 (CEST)

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