Phenotype #0000001830

Individual ID 00002674
Associated disease CMYO6;MYPOP
Phenotype details autosomal dominant inclusion body myopathy, joint contractures, ophthalmoplegia, rimmed vacuoles
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license No license selected
Created by Johan den Dunnen
Date created 2013-09-19 18:49:34 +02:00 (CEST)
Date last edited N/A

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