Charcot-Marie-Tooth disease type 2
MONDO:0018993A Charcot-Marie-Tooth disease characterized by abnormalities in the axon of the peripheral nerve cell.
Also known as: CMT2, autosomal dominant axonal Charcot-Marie-Tooth disease, hereditary motor and sensory neuropathy type 2, Charcot-Marie-Tooth type 2, autosomal dominant Charcot-Marie-Tooth disease type 2
16 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Charcot-Marie-Tooth disease axonal type 2S
(2)
Charcot-Marie-Tooth disease type 2A1
(1)
Charcot-Marie-Tooth disease type 2A2
(1)
Charcot-Marie-Tooth disease type 2D
(1)
Charcot-Marie-Tooth disease type 2J
(1)
Autosomal dominant charcot-marie-tooth disease type 2 due to DGAT2 mutation
(0)
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
(0)
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation
(0)
Autosomal dominant Charcot-Marie-Tooth disease type 2K
(0)
Autosomal dominant Charcot-Marie-Tooth disease type 2M
(0)
Autosomal dominant Charcot-Marie-Tooth disease type 2W
(0)
Charcot-Marie-Tooth disease axonal type 2C
(0)
Charcot-Marie-Tooth disease axonal type 2CC
(0)
Charcot-Marie-tooth disease, axonal, type 2DD
(0)
Charcot-Marie-Tooth disease, axonal, type 2EE
(0)
Charcot-Marie-Tooth disease axonal type 2F
(0)
Charcot-Marie-Tooth disease axonal type 2H
(0)
Charcot-Marie-Tooth disease axonal type 2K
(0)
Charcot-Marie-Tooth disease axonal type 2L
(0)
Charcot-Marie-Tooth disease axonal type 2N
(0)