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CMT2 (medical condition): A rare inherited disorder characterized by abnormalities in the axon of...more »
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list CMT2 as a "rare disease".
Source - Orphanet
CMT2: Another name for Charcot-Marie-Tooth disease, type 2 (or close medical condition association).
»Introduction: Charcot-Marie-Tooth disease, type 2
»Symptoms of Charcot-Marie-Tooth disease, type 2
CMT2: CMT2 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of CMT2 incude:
Search to find out more about CMT2:
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