ONKI3 | Medical Subject Headings

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Hereditary Central Nervous System Demyelinating Diseases

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Heredodegenerative Disorders, Nervous System ∟ Hereditary Central Nervous System Demyelinating Diseases 31 coordinate concepts 6 subordinate concepts ∟ Adrenoleukodystrophy \| ∟ Alexander Disease \| ∟ Canavan Disease \| ∟ Leukodystrophy, Globoid Cell \| ∟ Leukodystrophy, Metachromatic \| ∟ Pelizaeus-Merzbacher Disease ∟ Alexander Disease \| ∟ Amyloid Neuropathies, Familial \| ∟ Canavan Disease \| ∟ Cockayne Syndrome \| ∟ Dystonia Musculorum Deformans \| ∟ Gerstmann-Straussler-Scheinker Disease \| ∟ Hallervorden-Spatz Syndrome \| ∟ Hepatolenticular Degeneration \| ∟ Hereditary Motor and Sensory Neuropathies \| ∟ Hereditary Sensory and Autonomic Neuropathies \| ∟ 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 \| ∟ Demyelinating Autoimmune Diseases, CNS \| ∟ Leukoencephalopathy, Progressive Multifocal \| ∟ Myelinolysis, Central Pontine \| ∟ Polyradiculoneuropathy \| ∟ Subacute Combined Degeneration Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Demyelinating Diseases ∟ Hereditary Central Nervous System Demyelinating Diseases 31 coordinate concepts 6 subordinate concepts ∟ Adrenoleukodystrophy \| ∟ Alexander Disease \| ∟ Canavan Disease \| ∟ Leukodystrophy, Globoid Cell \| ∟ Leukodystrophy, Metachromatic \| ∟ Pelizaeus-Merzbacher Disease ∟ Alexander Disease \| ∟ Amyloid Neuropathies, Familial \| ∟ Canavan Disease \| ∟ Cockayne Syndrome \| ∟ Dystonia Musculorum Deformans \| ∟ Gerstmann-Straussler-Scheinker Disease \| ∟ Hallervorden-Spatz Syndrome \| ∟ Hepatolenticular Degeneration \| ∟ Hereditary Motor and Sensory Neuropathies \| ∟ Hereditary Sensory and Autonomic Neuropathies \| ∟ 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 \| ∟ Demyelinating Autoimmune Diseases, CNS \| ∟ Leukoencephalopathy, Progressive Multifocal \| ∟ Myelinolysis, Central Pontine \| ∟ Polyradiculoneuropathy \| ∟ Subacute Combined Degeneration Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurodegenerative Diseases ∟ Heredodegenerative Disorders, Nervous System ∟ Hereditary Central Nervous System Demyelinating Diseases 31 coordinate concepts 6 subordinate concepts ∟ Adrenoleukodystrophy \| ∟ Alexander Disease \| ∟ Canavan Disease \| ∟ Leukodystrophy, Globoid Cell \| ∟ Leukodystrophy, Metachromatic \| ∟ Pelizaeus-Merzbacher Disease ∟ Alexander Disease \| ∟ Amyloid Neuropathies, Familial \| ∟ Canavan Disease \| ∟ Cockayne Syndrome \| ∟ Dystonia Musculorum Deformans \| ∟ Gerstmann-Straussler-Scheinker Disease \| ∟ Hallervorden-Spatz Syndrome \| ∟ Hepatolenticular Degeneration \| ∟ Hereditary Motor and Sensory Neuropathies \| ∟ Hereditary Sensory and Autonomic Neuropathies \| ∟ 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 \| ∟ Demyelinating Autoimmune Diseases, CNS \| ∟ Leukoencephalopathy, Progressive Multifocal \| ∟ Myelinolysis, Central Pontine \| ∟ Polyradiculoneuropathy \| ∟ Subacute Combined Degeneration X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Heredodegenerative Disorders, Nervous System ∟ Hereditary Central Nervous System Demyelinating Diseases Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Demyelinating Diseases ∟ Hereditary Central Nervous System Demyelinating Diseases Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurodegenerative Diseases ∟ Heredodegenerative Disorders, Nervous System ∟ Hereditary Central Nervous System Demyelinating Diseases Heredodegenerative Disorders, Nervous System > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Demyelinating Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Heredodegenerative Disorders, Nervous System > Neurodegenerative Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Adrenoleukodystrophy \| Alexander Disease \| Canavan Disease \| Leukodystrophy, Globoid Cell \| Leukodystrophy, Metachromatic \| Pelizaeus-Merzbacher Disease X
historyNote*:	2000 X
publicMeSHNote*:	2000 X
Scope note:	Inherited conditions characterized by a loss of myelin in the central nervous system. X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-11-03X
dateEstablished*:	2000-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	KEVX
Type:	Concept X
Coordinate terms:	Alexander Disease \| Amyloid Neuropathies, Familial \| Canavan Disease \| Cockayne Syndrome \| Dystonia Musculorum Deformans \| Gerstmann-Straussler-Scheinker Disease \| Hallervorden-Spatz Syndrome \| Hepatolenticular Degeneration \| Hereditary Motor and Sensory Neuropathies \| Hereditary Sensory and Autonomic Neuropathies \| 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 \| Demyelinating Autoimmune Diseases, CNS \| Leukoencephalopathy, Progressive Multifocal \| Myelinolysis, Central Pontine \| Polyradiculoneuropathy \| Subacute Combined Degeneration X
URI:	X
Labels and equivalent concepts:	Keskushermoston perinnölliset demyelinisoivat sairaudet (fi) Ärfliga demyeliniserande sjukdomar i det centrala nervsystemet (sv) Demyelinating Diseases, Central Nervous System, Hereditary (en, replaced) Hereditary Demyelinating Diseases, Central Nervous System (en, replaced) Demyelinating Central Nervous System Diseases, Hereditary (en, replaced) Central Nervous System Hereditary Demyelinating Diseases (en, replaced) Central Nervous System Demyelinating Hereditary Diseases (en, replaced) Central Nervous System Demyelinating Diseases, Hereditary (en, replaced) X
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