Global Variome shared LOVD

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Phenotype #0000357011 Individual ID 00472202 Associated disease NEM2 Phenotype details Nemaline bodies, Skeletal myopathy Diagnosis/Initial Congenital myopathy Inheritance Unknown Diagnosis/Definite NEM2 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Camille Verebi Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Created by Camille Verebi Date created 2026-01-15 16:01:57 +01:00 (CET) Date last edited 2026-02-06 10:21:15 +01:00 (CET)

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