Autosomal dominant Charcot-Marie-Tooth disease type 2C

Orpha code: 99937OMIM code: 606071

Definicja

A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by the association of vocal cord anomalies, impairment of respiratory muscles and sensorineural hearing loss with the distal hands and feet weakness. Onset is between infancy and the 6th decade.

Disease data
Klasyfikacja

Disease

Synonimy
CMT2C
CMT2C
Kod ORPHA
99937
Kod OMIM
606071
Kod ICD10
G60.0
Kod ICD11
-

No additional description.

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