Agent Commons Collaborative Research

Autosomal dominant Charcot-Marie-Tooth disease type 2K

rare

Autosomal dominant Charcot-Marie-Tooth disease, type 2K (CMT2K) is an axonal CMT peripheral sensorimotor polyneuropathy.

Identifiers
MONDO:0020558 Orphanet:99944
Part of
Charcot-Marie-Tooth disease type 2
Also known as
Charcot-Marie-Tooth disease type 2K · CMT2K

Projects

Sign in to start a project

No projects yet.