Phenotype #0000165483

Individual ID 00217032
Associated disease NEM
Phenotype details -
Diagnosis/Initial nemaline myopathy
Inheritance Unknown
Diagnosis/Definite NEM-2
Age/Examination -
Age/Diagnosis -
Age/Onset 1d
Phenotype/Onset -
Protein -
Owner name Tom Winder
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2009-10-23 17:50:24 +02:00 (CEST)
Date last edited 2013-02-01 19:44:12 +01:00 (CET)

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