Global Variome shared LOVD

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

Phenotype #0000291750 Individual ID 00398667 Associated disease CMT4C Phenotype details Demyelinating peripheral neuropathy (HP:0007108), Decreased nerve conduction velocity (HP:0000762) Diagnosis/Initial CMT Inheritance Familial, autosomal recessive Diagnosis/Definite CMT4C Age/Examination 45y (45 years) Age/Diagnosis - Age/Onset 20y Phenotype/Onset Demyelinating peripheral neuropathy (HP:0007108), Decreased nerve conduction velocity (HP:0000762) Protein - Owner name Yvet den Hartog Database submission license Creative Commons Attribution 4.0 International Created by Yvet den Hartog Date created 2022-01-09 11:51:30 +01:00 (CET) Date last edited 2022-01-18 16:05:58 +01:00 (CET)

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