Global Variome shared LOVD

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Phenotype #0000153537 Individual ID 00205343 Associated disease CMS Phenotype details - Diagnosis/Initial congenital myasthenic syndrome Inheritance Unknown Diagnosis/Definite CMS-5 Age/Examination - Age/Diagnosis - Age/Onset 0d Phenotype/Onset ptosis, intermittent squint, hypotonia, slow feeding Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2011-11-20 17:57:20 +01:00 (CET) Date last edited 2013-02-01 19:44:08 +01:00 (CET)

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