Phenotype #0000106558

Individual ID 00133809
Associated disease LGMD
Phenotype details >9y-inable to walk (HP:0002540)
Diagnosis/Initial dystrophy, muscular, limb-girdle (LGMD)
Inheritance Unknown
Diagnosis/Definite LGMD2C
Age/Examination -
Age/Diagnosis -
Age/Onset 6y
Phenotype/Onset -
Protein IHC no SGCG, severly reduced SGCA, reduced DMD, SGCB and SGCD
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 2007-07-13 16:38:45 +02:00 (CEST)
Date last edited 2020-10-04 11:07:05 +02:00 (CEST)

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