Global Variome shared LOVD

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

Phenotype #0000124225 Individual ID 00151862 Associated disease CMT Phenotype details early-onset demyelinating neuropathy Diagnosis/Initial Charcot-Marie-Tooth disease (CMT) Inheritance Familial, autosomal recessive Diagnosis/Definite CMT-4H 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 2012-11-05 15:13:21 +01:00 (CET) Date last edited 2018-01-27 16:32:29 +01:00 (CET)

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