Global Variome shared LOVD

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

Phenotype #0000155390 Individual ID 00207579 Associated disease CMT Phenotype details sensori-motor demyelinating neuropathy in the lower limbs, scoliosis Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite CMT4C Age/Examination 29y (29 years) Age/Diagnosis 29y Age/Onset 06y Phenotype/Onset ? Protein SH3TC2 Owner name Justine Lerat Database submission license No license selected Created by Justine Lerat Date created 2018-11-25 17:51:38 +01:00 (CET) Date last edited 2018-12-03 14:48:55 +01:00 (CET)

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