Phenotype #0000165575

Individual ID 00217124
Associated disease NEM
Phenotype details severe
Diagnosis/Initial nemaline myopathy
Inheritance Isolated (sporadic)
Diagnosis/Definite NEM-2
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 2014-06-06 15:26:46 +02:00 (CEST)
Date last edited N/A

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