Global Variome shared LOVD

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

Phenotype #0000165782 Individual ID 00217332 Associated disease CCD Phenotype details delayed motor development, ptosis, strabismus, scoliosis, amyotrophy Diagnosis/Initial central core disease Inheritance Unknown Diagnosis/Definite CCD Age/Examination - Age/Diagnosis - Age/Onset 1d Phenotype/Onset Hydramnion, fetal akinesia Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2009-11-01 22:02:20 +01:00 (CET) Date last edited 2013-02-01 19:44:12 +01:00 (CET)

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