Autosomal dominant Charcot-Marie-Tooth disease type 2A1
|
(Orphanet:99946)
|
Autosomal dominant Charcot-Marie-Tooth disease type 2A2
|
(Orphanet:99947)
|
Autosomal dominant Charcot-Marie-Tooth disease type 2B
|
(Orphanet:99936)
|
Autosomal dominant Charcot-Marie-Tooth disease type 2C
|
(Orphanet:99937)
|
Autosomal dominant Charcot-Marie-Tooth disease type 2D
|
(Orphanet:99938)
|
Autosomal dominant Charcot-Marie-Tooth disease type 2E
|
(Orphanet:99939)
|
Autosomal dominant Charcot-Marie-Tooth disease type 2F
|
(Orphanet:99940)
|
Autosomal dominant Charcot-Marie-Tooth disease type 2G
|
(Orphanet:99941)
|
Autosomal dominant Charcot-Marie-Tooth disease type 2I
|
(Orphanet:99942)
|
Autosomal dominant Charcot-Marie-Tooth disease type 2J
|
(Orphanet:99943)
|
Autosomal dominant Charcot-Marie-Tooth disease type 2K
|
(Orphanet:99944)
|
Autosomal dominant Charcot-Marie-Tooth disease type 2L
|
(Orphanet:99945)
|
Autosomal dominant Charcot-Marie-Tooth disease type 2M
|
(Orphanet:228179)
|
Autosomal dominant Charcot-Marie-Tooth disease type 2N
|
(Orphanet:228174)
|
Autosomal dominant Charcot-Marie-Tooth disease type 2O
|
(Orphanet:284232)
|
Autosomal dominant Charcot-Marie-Tooth disease type 2P
|
(Orphanet:300319)
|
Autosomal dominant intermediate Charcot-Marie-Tooth disease type A
|
(Orphanet:100043)
|
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
|
(Orphanet:100044)
|
Autosomal dominant intermediate Charcot-Marie-Tooth disease type C
|
(Orphanet:100045)
|
Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
|
(Orphanet:100046)
|
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
|
(Orphanet:93114)
|
Autosomal recessive intermediate Charcot-Marie-Tooth disease type C
|
(Orphanet:369867)
|
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE
|
(OMIM:607706)
|
Charcot-Marie-Tooth disease type 1A
|
(Orphanet:101081)
|
Charcot-Marie-Tooth disease type 1B
|
(Orphanet:101082)
|
Charcot-Marie-Tooth disease type 1C
|
(Orphanet:101083)
|
Charcot-Marie-Tooth disease type 1D
|
(Orphanet:101084)
|
Charcot-Marie-Tooth disease type 1E
|
(Orphanet:90658)
|
Charcot-Marie-Tooth disease type 1F
|
(Orphanet:101085)
|
Charcot-Marie-Tooth disease type 2B1
|
(Orphanet:98856)
|
Charcot-Marie-Tooth disease type 2B2
|
(Orphanet:101101)
|
Charcot-Marie-Tooth disease type 2H
|
(Orphanet:101102)
|
Charcot-Marie-Tooth disease type 4A
|
(Orphanet:99948)
|
Charcot-Marie-Tooth disease type 4B1
|
(Orphanet:99955)
|
Charcot-Marie-Tooth disease type 4B2
|
(Orphanet:99956)
|
Charcot-Marie-Tooth disease type 4D
|
(Orphanet:99950)
|
Charcot-Marie-Tooth disease type 4E
|
(Orphanet:99951)
|
Dejerine-Sottas syndrome
|
(Orphanet:64748)
|
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT
|
(OMIM:610100)
|
Giant axonal neuropathy
|
(Orphanet:643)
|
Hereditary motor and sensory neuropathy type 5
|
(Orphanet:64751)
|
Hereditary motor and sensory neuropathy type 6
|
(Orphanet:90120)
|
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA
|
(OMIM:600794)
|
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA
|
(OMIM:158580)
|
Roussy-Lévy syndrome
|
(Orphanet:3115)
|
X-linked Charcot-Marie-Tooth disease type 1
|
(Orphanet:101075)
|
X-linked Charcot-Marie-Tooth disease type 3
|
(Orphanet:101077)
|
X-linked Charcot-Marie-Tooth disease type 5
|
(Orphanet:99014)
|