Autosomal dominant Charcot-Marie-Tooth disease type 2G

Orpha code: 99941OMIM code: 614436

Definicja

A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy with onset associated to development of foot deformity and walking difficulties between the 1st and the 8th decades, with a median range in the 2nd one. Weakness and sensory loss involve primarily the legs and ankles tendon reflexes are reduced. This disorder has a slowly progressive course.

Disease data
Klasyfikacja

Disease

Synonimy
CMT2G
CMT2G
Kod ORPHA
99941
Kod OMIM
614436
Kod ICD10
G60.0
Kod ICD11
-

No additional description.

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