ORPHA:284232 Classification level: Disorder Synonym(s): CMT2O Prevalence: 1 / 1 000 000 Inheritance: Autosomal dominant Age of onset: Childhood ICD-10: G60.0 OMIM: 614228 UMLS: - MeSH: - GARD: 12434 MedDRA: - The documents contained in this web site are presented [orpha.net]

The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. [orpha.net]