Phenotype #0000139643
Individual ID |
00174816 |
Associated disease |
LGMD |
Phenotype details |
onset overt symptoms childhood; CPK raised 33x; limb-girdle weakness, waddling gait; improvement after corticosteroid treatment; Mi2-antibodies |
Diagnosis/Initial |
proximal myopathy |
Inheritance |
Isolated (sporadic) |
Diagnosis/Definite |
- |
Age/Examination |
06y (6 years) |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2018-08-10 19:10:48 +02:00 (CEST) |
Date last edited |
2020-02-10 15:53:14 +01:00 (CET) |
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