Global Variome shared LOVD

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Phenotype #0000042966 Individual ID 00056353 Associated disease CNM1 Phenotype details early onset; neonatal hypotonia, stable muscle involvement, ophthalmoparesis Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2010-05-30 22:33:42 +02:00 (CEST) Date last edited 2012-03-10 10:47:48 +01:00 (CET)

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