Phenotype #0000139569

Individual ID 00174742
Associated disease LGMD
Phenotype details onset overt symptoms early adulthood; CPK raised 23x; myalgia, exercise intolerance, fatigability; mild generalized muscle hypertrophy, calf asymmetry; minimal weakness, ambulation normal
Diagnosis/Initial limb-girdle muscular dystrophy
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination 22y (22 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
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 2018-08-10 19:10:48 +02:00 (CEST)
Date last edited N/A

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