Charcot-Marie-Tooth disease

MONDO:0015626

An inherited degenerative disorder involving the peripheral nerves. It is caused by mutations in the genes that are responsible for the production of proteins necessary for the function and structure of the peripheral nerves. It is characterized by muscle atrophy and weakness in the feet, legs, hands, and arms and loss of sensation in the limbs.

Also known as: hereditary motor and sensory neuropathy, hereditary sensorimotor neuropathy, CMT, CMT/HMSN, Charcot Marie Tooth muscular atrophy, Charcot-Marie-Tooth disease, Charcot-Marie-Tooth hereditary neuropathy, peroneal muscular atrophy

83 clinical trials for this condition and its sub-types, 52 tagged with Charcot-Marie-Tooth disease itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Hereditary peripheral neuropathy (479)

Sub-types of Charcot-Marie-Tooth disease

Charcot-Marie-Tooth disease type 1 4 trials · 40 incl. sub-types
6 sub-types
- Charcot-Marie-Tooth disease type 1F 21 trials
- Charcot-Marie-Tooth disease type 1A 16 trials
- Charcot-Marie-Tooth disease type 1B 3 trials
- Charcot-Marie-Tooth disease type 1C 1 trial
- Charcot-Marie-Tooth disease type 1D 1 trial
- Charcot-Marie-Tooth disease type 1E 1 trial
Charcot-Marie-Tooth disease type 2 3 trials · 9 incl. sub-types
39 sub-types
- Charcot-Marie-Tooth disease axonal type 2S 3 trials
- Charcot-Marie-Tooth disease type 2A1 2 trials
- Charcot-Marie-Tooth disease type 2A2 2 trials
- Charcot-Marie-Tooth disease type 2D 2 trials
- Charcot-Marie-Tooth disease type 2J 2 trials
- Charcot-Marie-Tooth disease axonal type 2C 1 trial
- Charcot-Marie-Tooth disease axonal type 2H 1 trial
- Charcot-Marie-Tooth disease axonal type 2L 1 trial
- Charcot-Marie-Tooth disease axonal type 2N 1 trial
- Charcot-Marie-Tooth disease axonal type 2O 1 trial
- Charcot-Marie-Tooth disease axonal type 2P 1 trial
- Charcot-Marie-Tooth disease axonal type 2Q 1 trial
- Charcot-Marie-Tooth disease axonal type 2U 1 trial
- Charcot-Marie-Tooth disease type 2B1 1 trial
- Charcot-Marie-Tooth disease type 2B2 1 trial
- Charcot-Marie-Tooth disease type 2B5 1 trial
- Charcot-Marie-Tooth disease type 2E 1 trial
- Charcot-Marie-Tooth disease type 2I 1 trial
- Charcot-Marie-Tooth disease type 2R 1 trial
- Charcot-Marie-Tooth disease type 2T 1 trial
- Charcot-Marie-Tooth disease type 2Y 1 trial
- Autosomal dominant Charcot-Marie-Tooth disease type 2K 1 trial
- Autosomal dominant Charcot-Marie-Tooth disease type 2M 1 trial
- Charcot-Marie-Tooth disease axonal type 2CC 0 trials
- Charcot-Marie-Tooth disease axonal type 2F 0 trials
- Charcot-Marie-Tooth disease axonal type 2K 0 trials
- Charcot-Marie-Tooth disease axonal type 2T 0 trials
- Charcot-Marie-Tooth disease axonal type 2V 0 trials
- Charcot-Marie-Tooth disease axonal type 2X 0 trials
- Charcot-Marie-Tooth disease axonal type 2Z 0 trials
- Charcot-Marie-Tooth disease type 2B 0 trials
- Charcot-Marie-Tooth disease, axonal, type 2EE 0 trials
- Charcot-Marie-tooth disease, axonal, type 2DD 0 trials
- MME-related autosomal dominant Charcot Marie Tooth disease type 2 0 trials
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation 0 trials
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation 0 trials
- Autosomal dominant Charcot-Marie-Tooth disease type 2W 0 trials
- Autosomal dominant charcot-marie-tooth disease type 2 due to DGAT2 mutation 0 trials
- Giant axonal neuropathy 2 0 trials
Charcot-Marie-Tooth disease type 4 0 trials · 5 incl. sub-types
12 sub-types
- Charcot-Marie-Tooth disease type 4J 3 trials
- Charcot-Marie-Tooth disease type 4A 2 trials
- Charcot-Marie-Tooth disease type 4B1 2 trials
- Charcot-Marie-Tooth disease type 4B2 2 trials
- Charcot-Marie-Tooth disease type 4C 2 trials
- Charcot-Marie-Tooth disease type 4D 2 trials
- Charcot-Marie-Tooth disease type 4B3 1 trial
- Charcot-Marie-Tooth disease type 4E 1 trial
- Charcot-Marie-Tooth disease type 4F 1 trial
- Charcot-Marie-Tooth disease type 4H 1 trial
- Charcot-Marie-Tooth disease type 4G 0 trials
- Charcot-Marie-Tooth disease type 4K 0 trials
Intermediate Charcot-Marie-Tooth disease 0 trials · 3 incl. sub-types
3 sub-types
- Autosomal dominant intermediate Charcot-Marie-Tooth disease 0 trials · 3 incl. sub-types Sub-types →
- Autosomal recessive intermediate Charcot-Marie-Tooth disease 0 trials · 2 incl. sub-types Sub-types →
- Charcot-Marie-Tooth disease, dominant intermediate G 0 trials
Charcot-Marie-Tooth disease type X 1 trial · 2 incl. sub-types
6 sub-types
- Charcot-Marie-Tooth disease X-linked dominant 1 1 trial
- Charcot-Marie-Tooth disease X-linked dominant 6 0 trials
- Charcot-Marie-Tooth disease X-linked recessive 2 0 trials
- Charcot-Marie-Tooth disease X-linked recessive 3 0 trials
- Charcot-Marie-Tooth disease X-linked recessive 4 0 trials
- Charcot-Marie-Tooth disease X-linked recessive 5 0 trials
Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b; 1 trial
Charcot-Marie-Tooth disease type 3 0 trials
Charcot-Marie-Tooth disease with ptosis and parkinsonism 0 trials
Charcot-Marie-Tooth disease, Guadalajara neuronal type 0 trials
Charcot-Marie-Tooth disease, axonal, IIa 2II 0 trials
Charcot-Marie-Tooth disease, axonal, Type 2HH 0 trials
Charcot-Marie-Tooth disease, axonal, mitochondrial form, 1 0 trials
Charcot-Marie-Tooth disease, axonal, type 2FF 0 trials
Charcot-Marie-Tooth disease, axonal, type 2KK 0 trials
Charcot-Marie-Tooth disease, axonal, type 2LL 0 trials
Charcot-Marie-Tooth disease, demyelinating, IIA 1H 0 trials
Charcot-Marie-Tooth disease, demyelinating, IIA 1I 0 trials
Charcot-Marie-Tooth disease, demyelinating, type 1G 0 trials
Charcot-Marie-Tooth disease, demyelinating, type 1J 0 trials
Charcot-Marie-tooth disease, axonal, type 2JJ 0 trials
Charcot-marie-tooth disease, axonal, type 2MM 0 trials
Demyelinating hereditary motor and sensory neuropathy 0 trials
Neuronopathy, distal hereditary motor, autosomal dominant 1 0 trials
Neuropathy, hereditary motor and sensory, type 6A 0 trials

Most studied deeper sub-types

Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive (1) Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain (0) Charcot-Marie-Tooth Disease, axonal, type 2GG (0) Charcot-Marie-Tooth disease, dominant intermediate A (0) Charcot-Marie-Tooth disease dominant intermediate B (0) Charcot-Marie-Tooth disease dominant intermediate C (0) Charcot-Marie-Tooth disease dominant intermediate D (0) Charcot-Marie-Tooth disease dominant intermediate E (0) Charcot-Marie-Tooth disease dominant intermediate F (0) Charcot-Marie-Tooth disease recessive intermediate A (0) Charcot-Marie-Tooth disease recessive intermediate B (0) Charcot-Marie-Tooth disease recessive intermediate C (0) Charcot-Marie-Tooth disease recessive intermediate D (0)

Including sub-types (83) Tagged with Charcot-Marie-Tooth disease (52)

Trials to join now! 28 Not yet recruiting 2 Not yet finished but already full! 3 Completed 18 Terminated 1

Charcot-Marie-Tooth disease

Where it sits in the disease tree

Most studied deeper sub-types

One-Patient trial hopes to fix rare nerve disease at its genetic root

Can a One-Time gene injection halt nerve damage in CMT1A?

Can wearable sensors and walking tests reliably track nerve damage?