ONKI3 | MedIEQ: Medical Subject Headings

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Charcot-Marie-Tooth Disease

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Nervous System Malformations ∟ Hereditary Motor and Sensory Neuropathies ∟ Charcot-Marie-Tooth Disease 2 coordinate concepts ∟ Refsum Disease \| ∟ Spastic Paraplegia, Hereditary Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Heredodegenerative Disorders, Nervous System ∟ Hereditary Motor and Sensory Neuropathies ∟ Charcot-Marie-Tooth Disease 2 coordinate concepts ∟ Refsum Disease \| ∟ Spastic Paraplegia, Hereditary Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Nervous System Malformations ∟ Hereditary Motor and Sensory Neuropathies ∟ Charcot-Marie-Tooth Disease 2 coordinate concepts ∟ Refsum Disease \| ∟ Spastic Paraplegia, Hereditary Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurodegenerative Diseases ∟ Heredodegenerative Disorders, Nervous System ∟ Hereditary Motor and Sensory Neuropathies ∟ Charcot-Marie-Tooth Disease 2 coordinate concepts ∟ Refsum Disease \| ∟ Spastic Paraplegia, Hereditary Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Peripheral Nervous System Diseases ∟ Polyneuropathies ∟ Hereditary Motor and Sensory Neuropathies ∟ Charcot-Marie-Tooth Disease 2 coordinate concepts ∟ Refsum Disease \| ∟ Spastic Paraplegia, Hereditary X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Nervous System Malformations ∟ Hereditary Motor and Sensory Neuropathies ∟ Charcot-Marie-Tooth Disease Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Heredodegenerative Disorders, Nervous System ∟ Hereditary Motor and Sensory Neuropathies ∟ Charcot-Marie-Tooth Disease Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Nervous System Malformations ∟ Hereditary Motor and Sensory Neuropathies ∟ Charcot-Marie-Tooth Disease Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurodegenerative Diseases ∟ Heredodegenerative Disorders, Nervous System ∟ Hereditary Motor and Sensory Neuropathies ∟ Charcot-Marie-Tooth Disease Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Peripheral Nervous System Diseases ∟ Polyneuropathies ∟ Hereditary Motor and Sensory Neuropathies ∟ Charcot-Marie-Tooth Disease Hereditary Motor and Sensory Neuropathies > Nervous System Malformations > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Hereditary Motor and Sensory Neuropathies > Heredodegenerative Disorders, Nervous System > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Hereditary Motor and Sensory Neuropathies > Nervous System Malformations > Nervous System Diseases > Medical Subject Headings (MeSH) Hereditary Motor and Sensory Neuropathies > Heredodegenerative Disorders, Nervous System > Neurodegenerative Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Hereditary Motor and Sensory Neuropathies > Polyneuropathies > Peripheral Nervous System Diseases > Neuromuscular Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) X
historyNote*:	2000(1966) X
publicMeSHNote*:	2000; see CHARCOT-MARIE DISEASE 1991-1999, see MUSCULAR ATROPHY, SPINAL 1988-1990, see MUSCULAR ATROPHY 1966-1987; for CHARCOT-MARIE-TOOTH DISEASE see CHARCOT-MARIE DISEASE 1991-1999 X
Scope note:	A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343) X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-11-08X
dateEstablished*:	1991-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	NLMX
Related term:	Myelin P0 Protein X
Type:	Concept X
Coordinate terms:	Refsum Disease \| Spastic Paraplegia, Hereditary X
URI:	X
Labels and equivalent concepts:	Charcot-Marie-Toothin tauti (fi) HMSN Type I (en, replaced) Muscular Atrophy, Peroneal (en, replaced) Neuropathy, Type I Hereditary Motor and Sensory (en, replaced) HMSN II (en, replaced) HMSN I (en, replaced) Hereditary Motor, and Sensory Neuropathy Type I (en, replaced) HMN Distal Type I (en, replaced) Neuropathy, Type II Hereditary Motor and Sensory (en, replaced) Peroneal Muscular Atrophy (en, replaced) Hereditary Motor and Sensory-Neuropathy Type II (en, replaced) Charcot-Marie-Tooth Disease, Type II (en, replaced) Charcot-Marie Disease (en, replaced) Charcot-Marie-Tooth Disease, Type I (en, replaced) Atrophy, Muscular, Peroneal (en, replaced) Enfermedad de Charcot-Marie-Tooth (es) Charcot-Marie-Tooth-Krankheit (de) Charcotova-Marieova-Toothova nemoc (cs) Neuropatía Motora y Sensorial Hereditaria Tipo II (es, replaced) NSMH Tipo I (es, replaced) Síndrome de Roussy-Levy (es, replaced) Neuropatía Motora y Sensorial Hereditaria Tipo I (es, replaced) HMSN Tipo II (es, replaced) Atrofia Fibular (es, replaced) Atrofia Muscular Fibular (es, replaced) Erbliche Typ II motorische und sensorische Neuropathie (de, replaced) HMSN Typ I (de, replaced) HMSN Typ II (de, replaced) Erbliche Typ I motorische und sensorische Neuropathie (de, replaced) Charcot-Marie-Krankheit (de, replaced) Charcotova-Marieova-Toothova nemoc - typ Ib (cs, replaced) Atrophie, muskuläre, peroneale (de, replaced) Muskuläre Atrophie, peroneale (de, replaced) Neuropathie, Typ I, erbliche motorische und sensorische (de, replaced) Roussy-Lévy-Syndrom (de, replaced) Neuropathie, Typ II, erbliche motorische und sensorische (de, replaced) Peroneale Muskelatrophie (de, replaced) Charcotova-Marieova-Toothova nemoc - typ Ia (cs, replaced) X
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