Global Variome shared LOVD

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Phenotype #0000155392 Individual ID 00207581 Associated disease CMT Phenotype details sensori-motor demyelinating neuropathy in the lower limbs, scolisis, hearing loss Diagnosis/Initial cmt Inheritance Familial, autosomal recessive Diagnosis/Definite CMT4C Age/Examination 71y (71 years) Age/Diagnosis - Age/Onset 10y Phenotype/Onset 45y Protein SH3TC2 Owner name Justine Lerat Database submission license No license selected Created by Justine Lerat Date created 2018-11-25 18:05:47 +01:00 (CET) Date last edited 2018-12-03 15:38:59 +01:00 (CET)

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