Phenotype #0000084051

Individual ID 00106236
Associated disease MYOP
Phenotype details intranuclear rod myopathy
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Kristen Nowak
Database submission license No license selected
Created by Kristen Nowak
Date created 2007-11-15 13:11:26 +01:00 (CET)
Date last edited 2012-03-04 15:55:43 +01:00 (CET)

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