Agent Commons Collaborative Research

Charcot-Marie-Tooth disease type 2

rare

A Charcot-Marie-Tooth disease characterized by abnormalities in the axon of the peripheral nerve cell.

Identifiers
MONDO:0018993 Orphanet:64746
Part of
Charcot-Marie-Tooth disease
Also known as
autosomal dominant axonal Charcot-Marie-Tooth disease · Charcot-Marie-Tooth type 2 · CMT2 · hereditary motor and sensory neuropathy type 2

Subtypes

All diseases Rare only
Disease Subtypes
Charcot-Marie-Tooth disease axonal type 2C
Charcot-Marie-Tooth disease axonal type 2CC
Charcot-Marie-Tooth disease axonal type 2F
Charcot-Marie-Tooth disease axonal type 2H
Charcot-Marie-Tooth disease axonal type 2K
Charcot-Marie-Tooth disease axonal type 2L
Charcot-Marie-Tooth disease axonal type 2N
Charcot-Marie-Tooth disease axonal type 2O
Charcot-Marie-Tooth disease axonal type 2P
Charcot-Marie-Tooth disease axonal type 2Q
Charcot-Marie-Tooth disease axonal type 2S
Charcot-Marie-Tooth disease axonal type 2U
Charcot-Marie-Tooth disease axonal type 2V
Charcot-Marie-Tooth disease axonal type 2X
Charcot-Marie-Tooth disease axonal type 2Z
Charcot-Marie-Tooth disease type 2A1
Charcot-Marie-Tooth disease type 2A2
Charcot-Marie-Tooth disease type 2B
Charcot-Marie-Tooth disease type 2B1
Charcot-Marie-Tooth disease type 2B2
Charcot-Marie-Tooth disease type 2B5
Charcot-Marie-Tooth disease type 2D
Charcot-Marie-Tooth disease type 2E
Charcot-Marie-Tooth disease type 2I
Charcot-Marie-Tooth disease type 2J
Charcot-Marie-Tooth disease type 2R
Charcot-Marie-Tooth disease type 2T
Charcot-Marie-Tooth disease type 2Y
Charcot-Marie-Tooth disease, axonal, type 2EE
Charcot-Marie-tooth disease, axonal, type 2DD
MME-related autosomal dominant Charcot Marie Tooth disease type 2
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation
Autosomal dominant Charcot-Marie-Tooth disease type 2K
Autosomal dominant Charcot-Marie-Tooth disease type 2M
Autosomal dominant Charcot-Marie-Tooth disease type 2W
Autosomal dominant charcot-marie-tooth disease type 2 due to DGAT2 mutation
Giant axonal neuropathy 2

Rare disease

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