Phenotype #0000161971

Individual ID 00213512
Associated disease NEM
Phenotype details slowly progressive proximal muscle atrophy, weakness, dysphagia, rigid spine, dilated cardiomyopathy, type 2 repiratory failure
Diagnosis/Initial nemaline myopathy
Inheritance Familial, autosomal dominant
Diagnosis/Definite NEM-4
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 2010-11-10 22:57:39 +01:00 (CET)
Date last edited 2012-03-04 15:57:58 +01:00 (CET)

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