Autosomal dominant Charcot-Marie-Tooth disease type 2I

Orpha code: 99942OMIM code: 607677

Definicja

A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by a late onset with severe sensory loss (paresthesia and hypoesthesia) associated with distal weakness, mainly of the legs, and absent or reduced deep tendon reflexes.

Disease data
Klasyfikacja

Disease

Synonimy
CMT2I
CMT2I
Kod ORPHA
99942
Kod OMIM
607677
Kod ICD10
G60.0
Kod ICD11
-

No additional description.

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