Global Variome shared LOVD

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

Phenotype #0000125873 Individual ID 00153164 Associated disease CMS Phenotype details congenital ptosis, ophthalmoplegia Diagnosis/Initial syndrome, myasthenic, congenital Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Tom Winder Database submission license No license selected Created by Tom Winder Date created 2011-11-16 17:40:23 +01:00 (CET) Date last edited 2012-03-04 15:56:04 +01:00 (CET)

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