Phenotype #0000161996

Individual ID 00213542
Associated disease NEM
Phenotype details distal weakness lowerlimbs; wheelchair bound >40y
Diagnosis/Initial nemaline myopathy
Inheritance Familial, autosomal dominant
Diagnosis/Definite NEM-4
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Minttu Marttila
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-08-28 12:28:19 +02:00 (CEST)
Date last edited 2013-08-31 16:36:37 +02:00 (CEST)

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