Global Variome shared LOVD

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

Phenotype #0000155391 Individual ID 00207580 Associated disease CMT Phenotype details sensori-motor demyelinating neuropathy, scoliosis, hearing loss Diagnosis/Initial cmt Inheritance Familial, autosomal recessive Diagnosis/Definite CMT4C Age/Examination 68y (68 years) Age/Diagnosis 60y Age/Onset 09y Phenotype/Onset 60y Protein SH3TC2 Owner name Justine Lerat Database submission license No license selected Created by Justine Lerat Date created 2018-11-25 18:00:31 +01:00 (CET) Date last edited 2018-12-03 15:38:02 +01:00 (CET)

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