Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000125729 Individual ID 00152995 Associated disease CMS Phenotype details - Diagnosis/Initial syndrome, myasthenic, congenital, slow channel (SCCMS) Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Angela Abicht Database submission license No license selected Created by Angela Abicht Date created 2011-12-28 11:54:56 +01:00 (CET) Date last edited 2013-01-27 10:22:45 +01:00 (CET)

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