Phenotype #0000106371

Individual ID 00133624
Associated disease LGMD
Phenotype details intermediate, no cardiac involvement; no respiratory involvement; no skeletal deformity; >25y-inable to walk (HP:0002540); 3358 (23y) elevated CPK (HP:0003236)
Diagnosis/Initial dystrophy, muscular, limb-girdle (LGMD)
Inheritance Unknown
Diagnosis/Definite LGMD2E
Age/Examination -
Age/Diagnosis -
Age/Onset 10y
Phenotype/Onset -
Protein WB SGCA severely reduced, SGCG absent, DAG1 absent, DMD slightly reduced/normal
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 2009-06-28 12:14:45 +02:00 (CEST)
Date last edited 2020-10-04 11:06:22 +02:00 (CEST)

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