Ontomatica – ChEMATIC (Wedge)

The current query selects 627 items in 56 groups, which could be too many to show at once. If you are sure you want to see them all, you can proceed to see the entire category, 'or select a more specific subcategory of "Charcot-Marie-Tooth Disease [MESH:D002607]" below.

Subcategories in Nervous System Diseases [MESH:D009422] > Neurodegenerative Diseases [MESH:D019636] > Heredodegenerative Disorders, Nervous System [MESH:D020271] > Hereditary Sensory and Motor Neuropathy [MESH:D015417] > Charcot-Marie-Tooth Disease [MESH:D002607]:
(jump to C - H - K - N - P)

- C -
Charcot Marie Tooth type 1 aplasia cutis congenita [MESH:C538077] (1)
Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k [MESH:C564325] (1)
Charcot-Marie-Tooth Disease, Axonal, Type 2A2 [MESH:C563757] (31)
Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)
Charcot-Marie-Tooth Disease, Axonal, Type 2n [MESH:C567653] (33)
Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)
Charcot-Marie-Tooth Disease, Dominant Intermediate A [MESH:C564702] (1)
Charcot-Marie-Tooth Disease, Dominant Intermediate B [MESH:C564703] (27)
Charcot-Marie-Tooth Disease, Dominant Intermediate C [MESH:C564257] (39)
Charcot-Marie-Tooth Disease, Dominant Intermediate D [MESH:C564333] (22)
Charcot-Marie-Tooth Disease, Foot Deformity of [MESH:C564179] (1)
Charcot-Marie-Tooth Disease, Guadalajara Neuronal Type [MESH:C566137] (1)
Charcot-Marie-Tooth Disease, Recessive Intermediate A [MESH:C564256] (14)
Charcot-Marie-Tooth Disease, Type 4H [MESH:C563740] (29)
Charcot-Marie-Tooth Disease, Type 4j [MESH:C566984] (18)
Charcot-Marie-Tooth Neuropathy, Dominant Intermediate B, with Neutropenia [MESH:C564704] (1)
Charcot-Marie-Tooth Neuropathy, Type 4B2, with Early-Onset Glaucoma [MESH:C565761] (1)
Charcot-Marie-Tooth Peroneal Muscular Atrophy and Friedreich Ataxia, Combined [MESH:C564446] (1)
Charcot-Marie-Tooth disease and deafness [MESH:C538078] (1)
Charcot-Marie-Tooth disease with ptosis and parkinsonism [MESH:C538079] (1)
Charcot-Marie-Tooth disease, Type 1C [MESH:C537984] (69)
Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)
Charcot-Marie-Tooth disease, Type 1E [MESH:C537986] (1)
Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)
Charcot-Marie-Tooth disease, Type 2A [MESH:C537988] (1)
Charcot-Marie-Tooth disease, Type 2B [MESH:C537989] (15)
Charcot-Marie-Tooth disease, Type 2B1 [MESH:C537990] (77)
Charcot-Marie-Tooth disease, Type 2B2 [MESH:C537991] (11)
Charcot-Marie-Tooth disease, Type 2C [MESH:C537992] (1)
Charcot-Marie-Tooth disease, Type 2D [MESH:C537993] (43)
Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)
Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)
Charcot-Marie-Tooth disease, Type 2G [MESH:C535414] (1)
Charcot-Marie-Tooth disease, Type 2H [MESH:C535415] (1)
Charcot-Marie-Tooth disease, Type 2I [MESH:C535416] (22)
Charcot-Marie-Tooth disease, Type 2J [MESH:C535417] (22)
Charcot-Marie-Tooth disease, Type 2K [MESH:C535418] (14)
Charcot-Marie-Tooth disease, Type 4A [MESH:C535419] (14)
Charcot-Marie-Tooth disease, Type 4A, axonal form [MESH:C539595] (1)
Charcot-Marie-Tooth disease, Type 4B1 [MESH:C535420] (16)
Charcot-Marie-Tooth disease, Type 4B2 [MESH:C535421] (10)
Charcot-Marie-Tooth disease, Type 4B2, with early-onset glaucoma [MESH:C535422] (1)
Charcot-Marie-Tooth disease, Type 4C [MESH:C535423] (7)
Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)
Charcot-Marie-Tooth disease, X-linked recessive, 2 [MESH:C535302] (1)
Charcot-Marie-Tooth disease, X-linked recessive, 3 [MESH:C535303] (1)
Charcot-Marie-Tooth disease, X-linked, 1 [MESH:C535919] (72)
Charcot-Marie-Tooth disease, dominant intermediate 1 [MESH:C535399] (1)
Charcot-Marie-Tooth disease, dominant intermediate 2 [MESH:C535400] (1)
Charcot-Marie-Tooth disease, dominant intermediate 3 [MESH:C535401] (1)
Cowchock syndrome [MESH:C536450] (1)

- H -
Hereditary Motor And Sensory Neuropathy, Type IIC [MESH:C565261] (39)

- K -
Keratoderma palmoplantar spastic paralysis [MESH:C536153] (1)

- N -
Neuropathy, Distal Hereditary Motor, Type IIA [MESH:C563561] (1)
Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)

- P -
Polyneuropathy, Mixed, of Early Onset [MESH:C564879] (1)