Phenotype #0000083982

Individual ID 00106167
Associated disease MYOP
Phenotype details dominant congenital myopthy; patients show generalized proximal weakness in early childhood; non-progressive
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 2007-11-09 14:05:52 +01:00 (CET)
Date last edited 2012-03-04 15:55:43 +01:00 (CET)

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