Phenotype #0000346125

Individual ID 00457666
Associated disease MYOP
Diagnosis/Initial congenital myopathy
Diagnosis/Definite LGMDR23
Phenotype details see paper; ..., myopathy; abnormal skeletal muscle morphology; muscle weakness; abnormal muscle physiology; abnormal joint physiology
Inheritance Familial, autosomal recessive
Age/Examination -
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 2024-11-15 17:35:43 +01:00 (CET)
Date last edited N/A

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