Phenotype #0000209371

Individual ID 00274428
Associated disease MD
Phenotype details proximal muscle weakness, facial muscle weakness, elongated face and ophthalmoplegia; muscle myopathic pattern; CK 35 IU/L; ECG or echo normal; no family history
Diagnosis/Initial muscular dystrophy
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis 32y
Age/Onset 2y
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 2019-12-30 09:59:36 +01:00 (CET)
Date last edited N/A

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