Phenotype #0000161970

Individual ID 00213511
Associated disease NEM
Phenotype details -
Diagnosis/Initial nemaline myopathy
Inheritance Unknown
Diagnosis/Definite NEM-4
Age/Examination -
Age/Diagnosis -
Age/Onset -
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 2010-10-15 21:59:21 +02:00 (CEST)
Date last edited 2013-02-01 19:44:13 +01:00 (CET)

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