Phenotype #0000165489

Individual ID 00217038
Associated disease NEM
Phenotype details -
Diagnosis/Initial nemaline myopathy
Inheritance Unknown
Diagnosis/Definite NEM-2
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein nemaline rods
Owner name Tom Winder
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2009-10-28 17:09:42 +01:00 (CET)
Date last edited 2013-02-01 19:44:12 +01:00 (CET)

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