ONKI3 | Medical Subject Headings

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Hereditary Motor and Sensory Neuropathies

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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 39 coordinate concepts 3 subordinate concepts ∟ Charcot-Marie-Tooth Disease \| ∟ Refsum Disease \| ∟ Spastic Paraplegia, Hereditary ∟ Alcoholic Neuropathy \| ∟ Hereditary Sensory and Autonomic Neuropathies \| ∟ Paraneoplastic Polyneuropathy \| ∟ POEMS Syndrome \| ∟ Polyradiculoneuropathy \| ∟ Tangier Disease \| ∟ Alexander Disease \| ∟ Amyloid Neuropathies, Familial \| ∟ Canavan Disease \| ∟ Cockayne Syndrome \| ∟ Dystonia Musculorum Deformans \| ∟ Gerstmann-Straussler-Scheinker Disease \| ∟ Hallervorden-Spatz Syndrome \| ∟ Hepatolenticular Degeneration \| ∟ Hereditary Central Nervous System Demyelinating Diseases \| ∟ Huntington Disease \| ∟ Lafora Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Myotonia Congenita \| ∟ Myotonic Dystrophy \| ∟ Neurofibromatoses \| ∟ Neuronal Ceroid-Lipofuscinoses \| ∟ Optic Atrophies, Hereditary \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome \| ∟ Central Nervous System Cysts \| ∟ Central Nervous System Vascular Malformations \| ∟ Dandy-Walker Syndrome \| ∟ Holoprosencephaly \| ∟ Hydranencephaly \| ∟ Intracranial Arteriovenous Malformations \| ∟ Neural Tube Defects \| ∟ Septo-Optic Dysplasia Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Heredodegenerative Disorders, Nervous System ∟ Hereditary Motor and Sensory Neuropathies 39 coordinate concepts 3 subordinate concepts ∟ Charcot-Marie-Tooth Disease \| ∟ Refsum Disease \| ∟ Spastic Paraplegia, Hereditary ∟ Alcoholic Neuropathy \| ∟ Hereditary Sensory and Autonomic Neuropathies \| ∟ Paraneoplastic Polyneuropathy \| ∟ POEMS Syndrome \| ∟ Polyradiculoneuropathy \| ∟ Tangier Disease \| ∟ Alexander Disease \| ∟ Amyloid Neuropathies, Familial \| ∟ Canavan Disease \| ∟ Cockayne Syndrome \| ∟ Dystonia Musculorum Deformans \| ∟ Gerstmann-Straussler-Scheinker Disease \| ∟ Hallervorden-Spatz Syndrome \| ∟ Hepatolenticular Degeneration \| ∟ Hereditary Central Nervous System Demyelinating Diseases \| ∟ Huntington Disease \| ∟ Lafora Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Myotonia Congenita \| ∟ Myotonic Dystrophy \| ∟ Neurofibromatoses \| ∟ Neuronal Ceroid-Lipofuscinoses \| ∟ Optic Atrophies, Hereditary \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome \| ∟ Central Nervous System Cysts \| ∟ Central Nervous System Vascular Malformations \| ∟ Dandy-Walker Syndrome \| ∟ Holoprosencephaly \| ∟ Hydranencephaly \| ∟ Intracranial Arteriovenous Malformations \| ∟ Neural Tube Defects \| ∟ Septo-Optic Dysplasia Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Nervous System Malformations ∟ Hereditary Motor and Sensory Neuropathies 39 coordinate concepts 3 subordinate concepts ∟ Charcot-Marie-Tooth Disease \| ∟ Refsum Disease \| ∟ Spastic Paraplegia, Hereditary ∟ Alcoholic Neuropathy \| ∟ Hereditary Sensory and Autonomic Neuropathies \| ∟ Paraneoplastic Polyneuropathy \| ∟ POEMS Syndrome \| ∟ Polyradiculoneuropathy \| ∟ Tangier Disease \| ∟ Alexander Disease \| ∟ Amyloid Neuropathies, Familial \| ∟ Canavan Disease \| ∟ Cockayne Syndrome \| ∟ Dystonia Musculorum Deformans \| ∟ Gerstmann-Straussler-Scheinker Disease \| ∟ Hallervorden-Spatz Syndrome \| ∟ Hepatolenticular Degeneration \| ∟ Hereditary Central Nervous System Demyelinating Diseases \| ∟ Huntington Disease \| ∟ Lafora Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Myotonia Congenita \| ∟ Myotonic Dystrophy \| ∟ Neurofibromatoses \| ∟ Neuronal Ceroid-Lipofuscinoses \| ∟ Optic Atrophies, Hereditary \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome \| ∟ Central Nervous System Cysts \| ∟ Central Nervous System Vascular Malformations \| ∟ Dandy-Walker Syndrome \| ∟ Holoprosencephaly \| ∟ Hydranencephaly \| ∟ Intracranial Arteriovenous Malformations \| ∟ Neural Tube Defects \| ∟ Septo-Optic Dysplasia Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurodegenerative Diseases ∟ Heredodegenerative Disorders, Nervous System ∟ Hereditary Motor and Sensory Neuropathies 39 coordinate concepts 3 subordinate concepts ∟ Charcot-Marie-Tooth Disease \| ∟ Refsum Disease \| ∟ Spastic Paraplegia, Hereditary ∟ Alcoholic Neuropathy \| ∟ Hereditary Sensory and Autonomic Neuropathies \| ∟ Paraneoplastic Polyneuropathy \| ∟ POEMS Syndrome \| ∟ Polyradiculoneuropathy \| ∟ Tangier Disease \| ∟ Alexander Disease \| ∟ Amyloid Neuropathies, Familial \| ∟ Canavan Disease \| ∟ Cockayne Syndrome \| ∟ Dystonia Musculorum Deformans \| ∟ Gerstmann-Straussler-Scheinker Disease \| ∟ Hallervorden-Spatz Syndrome \| ∟ Hepatolenticular Degeneration \| ∟ Hereditary Central Nervous System Demyelinating Diseases \| ∟ Huntington Disease \| ∟ Lafora Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Myotonia Congenita \| ∟ Myotonic Dystrophy \| ∟ Neurofibromatoses \| ∟ Neuronal Ceroid-Lipofuscinoses \| ∟ Optic Atrophies, Hereditary \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome \| ∟ Central Nervous System Cysts \| ∟ Central Nervous System Vascular Malformations \| ∟ Dandy-Walker Syndrome \| ∟ Holoprosencephaly \| ∟ Hydranencephaly \| ∟ Intracranial Arteriovenous Malformations \| ∟ Neural Tube Defects \| ∟ Septo-Optic Dysplasia Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Peripheral Nervous System Diseases ∟ Polyneuropathies ∟ Hereditary Motor and Sensory Neuropathies 39 coordinate concepts 3 subordinate concepts ∟ Charcot-Marie-Tooth Disease \| ∟ Refsum Disease \| ∟ Spastic Paraplegia, Hereditary ∟ Alcoholic Neuropathy \| ∟ Hereditary Sensory and Autonomic Neuropathies \| ∟ Paraneoplastic Polyneuropathy \| ∟ POEMS Syndrome \| ∟ Polyradiculoneuropathy \| ∟ Tangier Disease \| ∟ Alexander Disease \| ∟ Amyloid Neuropathies, Familial \| ∟ Canavan Disease \| ∟ Cockayne Syndrome \| ∟ Dystonia Musculorum Deformans \| ∟ Gerstmann-Straussler-Scheinker Disease \| ∟ Hallervorden-Spatz Syndrome \| ∟ Hepatolenticular Degeneration \| ∟ Hereditary Central Nervous System Demyelinating Diseases \| ∟ Huntington Disease \| ∟ Lafora Disease \| ∟ Lesch-Nyhan Syndrome \| ∟ Menkes Kinky Hair Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Myotonia Congenita \| ∟ Myotonic Dystrophy \| ∟ Neurofibromatoses \| ∟ Neuronal Ceroid-Lipofuscinoses \| ∟ Optic Atrophies, Hereditary \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome \| ∟ Central Nervous System Cysts \| ∟ Central Nervous System Vascular Malformations \| ∟ Dandy-Walker Syndrome \| ∟ Holoprosencephaly \| ∟ Hydranencephaly \| ∟ Intracranial Arteriovenous Malformations \| ∟ Neural Tube Defects \| ∟ Septo-Optic Dysplasia X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Nervous System Malformations ∟ Hereditary Motor and Sensory Neuropathies Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Heredodegenerative Disorders, Nervous System ∟ Hereditary Motor and Sensory Neuropathies Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Nervous System Malformations ∟ Hereditary Motor and Sensory Neuropathies Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurodegenerative Diseases ∟ Heredodegenerative Disorders, Nervous System ∟ Hereditary Motor and Sensory Neuropathies Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Peripheral Nervous System Diseases ∟ Polyneuropathies ∟ Hereditary Motor and Sensory Neuropathies Nervous System Malformations > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Heredodegenerative Disorders, Nervous System > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Nervous System Malformations > Nervous System Diseases > Medical Subject Headings (MeSH) Heredodegenerative Disorders, Nervous System > Neurodegenerative Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Polyneuropathies > Peripheral Nervous System Diseases > Neuromuscular Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Charcot-Marie-Tooth Disease \| Refsum Disease \| Spastic Paraplegia, Hereditary X
Annotation:	do not confuse with HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES; DF: NEUROPATHIES HEREDITARY MOTOR SENSORY X
History note:	Charcot-Marie Disease (1975-1988) \| Muscular Atrophy (1972-1988) \| Neuromuscular Diseases (1979-1988)X
historyNote*:	2000(1989) X
publicMeSHNote*:	2000; see NEUROPATHIES, HEREDITARY MOTOR AND SENSORY 1988-1999 X
Scope note:	A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-TOOTH DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343) X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2006A \| 2006B \| 2006C \| 2006D \| 2007X
dateCreated*:	1999-11-08X
dateEstablished*:	1988-01-01X
dateRevised*:	2005-07-28X
recordAuthorizer*:	agsX
recordMaintainer*:	agsX
recordOriginator*:	ECX
Type:	Concept X
Coordinate terms:	Alcoholic Neuropathy \| Hereditary Sensory and Autonomic Neuropathies \| Paraneoplastic Polyneuropathy \| POEMS Syndrome \| Polyradiculoneuropathy \| Tangier Disease \| Alexander Disease \| Amyloid Neuropathies, Familial \| Canavan Disease \| Cockayne Syndrome \| Dystonia Musculorum Deformans \| Gerstmann-Straussler-Scheinker Disease \| Hallervorden-Spatz Syndrome \| Hepatolenticular Degeneration \| Hereditary Central Nervous System Demyelinating Diseases \| Huntington Disease \| Lafora Disease \| Lesch-Nyhan Syndrome \| Menkes Kinky Hair Syndrome \| Mental Retardation, X-Linked \| Myotonia Congenita \| Myotonic Dystrophy \| Neurofibromatoses \| Neuronal Ceroid-Lipofuscinoses \| Optic Atrophies, Hereditary \| Rett Syndrome \| Spinal Muscular Atrophies of Childhood \| Spinocerebellar Degenerations \| Tourette Syndrome \| Tuberous Sclerosis \| Unverricht-Lundborg Syndrome \| Central Nervous System Cysts \| Central Nervous System Vascular Malformations \| Dandy-Walker Syndrome \| Holoprosencephaly \| Hydranencephaly \| Intracranial Arteriovenous Malformations \| Neural Tube Defects \| Septo-Optic Dysplasia X
URI:	X
Labels and equivalent concepts:	Perinnölliset motoriset ja sensoriset neuropatiat (fi) Hereditaariset motoriset ja sensoriset neuropatiat (fi, replaced) Periytyvät motoriset ja sensoriset neuropatiat (fi, replaced) Ärftliga motoriska och sensoriska nervsjukdomar (sv) Neuropathies, Hereditary Motor and Sensory (en, replaced) HMSN Type VII (en, replaced) Hereditary, Type III, Motor and Sensory Neuropathy (en, replaced) HMSN (en, replaced) Dejerine-Sottas Disease (en, replaced) X
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