ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Optic Atrophies, Hereditary

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Eye Diseases, Hereditary ∟ Optic Atrophies, Hereditary 35 coordinate concepts 3 subordinate concepts ∟ Optic Atrophy, Autosomal Dominant \| ∟ Optic Atrophy, Hereditary, Leber \| ∟ Wolfram Syndrome ∟ Albinism \| ∟ Aniridia \| ∟ Choroideremia \| ∟ Corneal Dystrophies, Hereditary \| ∟ Duane Retraction Syndrome \| ∟ Graves Ophthalmopathy \| ∟ Gyrate Atrophy \| ∟ Retinal Dysplasia \| ∟ Retinitis Pigmentosa \| ∟ 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 \| ∟ 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 \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Heredodegenerative Disorders, Nervous System ∟ Optic Atrophies, Hereditary 35 coordinate concepts 3 subordinate concepts ∟ Optic Atrophy, Autosomal Dominant \| ∟ Optic Atrophy, Hereditary, Leber \| ∟ Wolfram Syndrome ∟ Albinism \| ∟ Aniridia \| ∟ Choroideremia \| ∟ Corneal Dystrophies, Hereditary \| ∟ Duane Retraction Syndrome \| ∟ Graves Ophthalmopathy \| ∟ Gyrate Atrophy \| ∟ Retinal Dysplasia \| ∟ Retinitis Pigmentosa \| ∟ 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 \| ∟ 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 \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Eye Diseases, Hereditary ∟ Optic Atrophies, Hereditary 35 coordinate concepts 3 subordinate concepts ∟ Optic Atrophy, Autosomal Dominant \| ∟ Optic Atrophy, Hereditary, Leber \| ∟ Wolfram Syndrome ∟ Albinism \| ∟ Aniridia \| ∟ Choroideremia \| ∟ Corneal Dystrophies, Hereditary \| ∟ Duane Retraction Syndrome \| ∟ Graves Ophthalmopathy \| ∟ Gyrate Atrophy \| ∟ Retinal Dysplasia \| ∟ Retinitis Pigmentosa \| ∟ 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 \| ∟ 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 \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Optic Nerve Diseases ∟ Optic Atrophy ∟ Optic Atrophies, Hereditary 35 coordinate concepts 3 subordinate concepts ∟ Optic Atrophy, Autosomal Dominant \| ∟ Optic Atrophy, Hereditary, Leber \| ∟ Wolfram Syndrome ∟ Albinism \| ∟ Aniridia \| ∟ Choroideremia \| ∟ Corneal Dystrophies, Hereditary \| ∟ Duane Retraction Syndrome \| ∟ Graves Ophthalmopathy \| ∟ Gyrate Atrophy \| ∟ Retinal Dysplasia \| ∟ Retinitis Pigmentosa \| ∟ 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 \| ∟ 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 \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Cranial Nerve Diseases ∟ Optic Nerve Diseases ∟ Optic Atrophy ∟ Optic Atrophies, Hereditary 35 coordinate concepts 3 subordinate concepts ∟ Optic Atrophy, Autosomal Dominant \| ∟ Optic Atrophy, Hereditary, Leber \| ∟ Wolfram Syndrome ∟ Albinism \| ∟ Aniridia \| ∟ Choroideremia \| ∟ Corneal Dystrophies, Hereditary \| ∟ Duane Retraction Syndrome \| ∟ Graves Ophthalmopathy \| ∟ Gyrate Atrophy \| ∟ Retinal Dysplasia \| ∟ Retinitis Pigmentosa \| ∟ 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 \| ∟ 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 \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurodegenerative Diseases ∟ Heredodegenerative Disorders, Nervous System ∟ Optic Atrophies, Hereditary 35 coordinate concepts 3 subordinate concepts ∟ Optic Atrophy, Autosomal Dominant \| ∟ Optic Atrophy, Hereditary, Leber \| ∟ Wolfram Syndrome ∟ Albinism \| ∟ Aniridia \| ∟ Choroideremia \| ∟ Corneal Dystrophies, Hereditary \| ∟ Duane Retraction Syndrome \| ∟ Graves Ophthalmopathy \| ∟ Gyrate Atrophy \| ∟ Retinal Dysplasia \| ∟ Retinitis Pigmentosa \| ∟ 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 \| ∟ 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 \| ∟ Rett Syndrome \| ∟ Spinal Muscular Atrophies of Childhood \| ∟ Spinocerebellar Degenerations \| ∟ Tourette Syndrome \| ∟ Tuberous Sclerosis \| ∟ Unverricht-Lundborg Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Eye Diseases, Hereditary ∟ Optic Atrophies, Hereditary Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Heredodegenerative Disorders, Nervous System ∟ Optic Atrophies, Hereditary Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Eye Diseases, Hereditary ∟ Optic Atrophies, Hereditary Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Optic Nerve Diseases ∟ Optic Atrophy ∟ Optic Atrophies, Hereditary Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Cranial Nerve Diseases ∟ Optic Nerve Diseases ∟ Optic Atrophy ∟ Optic Atrophies, Hereditary Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurodegenerative Diseases ∟ Heredodegenerative Disorders, Nervous System ∟ Optic Atrophies, Hereditary Eye Diseases, Hereditary > Genetic Diseases, Inborn > 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) Eye Diseases, Hereditary > Eye Diseases > Medical Subject Headings (MeSH) Optic Atrophy > Optic Nerve Diseases > Eye Diseases > Medical Subject Headings (MeSH) Optic Atrophy > Optic Nerve Diseases > Cranial Nerve Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Heredodegenerative Disorders, Nervous System > Neurodegenerative Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Optic Atrophy, Autosomal Dominant \| Optic Atrophy, Hereditary, Leber \| Wolfram Syndrome X
History note:	Optic Atrophy/genetics (1966-1988)X
historyNote*:	2000(1989) X
publicMeSHNote*:	2000; see OPTIC ATROPHY, HEREDITARY 1991-1999, see NEUROPATHIES, HEREDITARY MOTOR AND SENSORY 1989-1990 X
Scope note:	Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER). X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1988-06-07X
dateEstablished*:	1991-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	ECX
Type:	Concept X
Coordinate terms:	Albinism \| Aniridia \| Choroideremia \| Corneal Dystrophies, Hereditary \| Duane Retraction Syndrome \| Graves Ophthalmopathy \| Gyrate Atrophy \| Retinal Dysplasia \| Retinitis Pigmentosa \| 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 \| 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 \| Rett Syndrome \| Spinal Muscular Atrophies of Childhood \| Spinocerebellar Degenerations \| Tourette Syndrome \| Tuberous Sclerosis \| Unverricht-Lundborg Syndrome X
URI:	X
Labels and equivalent concepts:	Perinnölliset näköhermon surkastumat (fi) Periytyvä näköhermon atrofia (fi, replaced) Perinnölliset optikusatrofiat (fi, replaced) Perinnölliset näköhermon atrofiat (fi, replaced) Periytyvä näköhermon surkastuma (fi, replaced) Periytyvä optikusatrofia (fi, replaced) Periytyvät optikusatrofiat (fi, replaced) Periytyvät näköhermon surkastumat (fi, replaced) Periytyvät näköhermon atrofiat (fi, replaced) Perinnöllinen optikusatrofia (fi, replaced) Perinnöllinen näköhermon surkastuma (fi, replaced) Hereditaarinen näköhermon surkastuma (fi, replaced) Hereditaarinen näköhermon atrofia (fi, replaced) Hereditaarinen optikusatrofia (fi, replaced) Hereditaariset näköhermon atrofiat (fi, replaced) Perinnöllinen näköhermon atrofia (fi, replaced) Hereditaariset optikusatrofiat (fi, replaced) Hereditaariset näköhermon surkastumat (fi, replaced) Optikusatrofier, ärftliga (sv) Optic Atrophy, Hereditary (en, replaced) Hereditary Optic Atrophy (en, replaced) X
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