Phenotype #0000106676

Individual ID 00133927
Associated disease LGMD2
Phenotype details -
Diagnosis/Initial dystrophy, muscular, limb-girdle, autosomal recessive, type 2 (LGMD-2)
Diagnosis/Definite dystrophy, muscular, limb-girdle, type 2C (LGMD-2C)
Inheritance Isolated (sporadic)
Age/Examination -
Age/Onset -
Phenotype/Onset -
Age/Diagnosis -
Protein WB no SGCA, no SGCG
Owner name Human Genetics Diagnostic Laboratory - Cochin Hosp J Chelly, F Leturcq
Database submission license No license selected
Created by Human Genetics Diagnostic Laboratory - Cochin Hosp J Chelly, F Leturcq
Date created 2008-10-12 17:35:30 +02:00 (CEST)
Date last edited 2012-03-09 18:58:40 +01:00 (CET)

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