Global Variome shared LOVD

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Phenotype #0000284026 Individual ID 00390489 Associated disease MDDG Phenotype details congenital muscular dystrophy, no mental retardation; 1y10m-walk, 3y1m-run; no contractures; no intellectual disability; no seizures; no eye involvement; CK level 15245 IU/L; MRI brain normal; muscle biopsy muscular dystrophy Diagnosis/Initial limb-girdle muscular dystrophy Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination 3y7m (3 years, 7 months) Age/Diagnosis - Age/Onset 4m 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 2021-11-10 16:44:31 +01:00 (CET) Date last edited N/A

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