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Spinocerebellar Ataxias

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Heredodegenerative Disorders, Nervous System ∟ Spinocerebellar Degenerations ∟ Spinocerebellar Ataxias 3 coordinate concepts 2 subordinate concepts ∟ Ataxia Telangiectasia \| ∟ Machado-Joseph Disease ∟ Friedreich Ataxia \| ∟ Myoclonic Cerebellar Dyssynergia \| ∟ Olivopontocerebellar Atrophies Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Cerebellar Diseases ∟ Cerebellar Ataxia ∟ Spinocerebellar Ataxias 3 coordinate concepts 2 subordinate concepts ∟ Ataxia Telangiectasia \| ∟ Machado-Joseph Disease ∟ Friedreich Ataxia \| ∟ Myoclonic Cerebellar Dyssynergia \| ∟ Olivopontocerebellar Atrophies Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Cerebellar Diseases ∟ Spinocerebellar Degenerations ∟ Spinocerebellar Ataxias 3 coordinate concepts 2 subordinate concepts ∟ Ataxia Telangiectasia \| ∟ Machado-Joseph Disease ∟ Friedreich Ataxia \| ∟ Myoclonic Cerebellar Dyssynergia \| ∟ Olivopontocerebellar Atrophies Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Spinal Cord Diseases ∟ Spinocerebellar Degenerations ∟ Spinocerebellar Ataxias 3 coordinate concepts 2 subordinate concepts ∟ Ataxia Telangiectasia \| ∟ Machado-Joseph Disease ∟ Friedreich Ataxia \| ∟ Myoclonic Cerebellar Dyssynergia \| ∟ Olivopontocerebellar Atrophies Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurodegenerative Diseases ∟ Heredodegenerative Disorders, Nervous System ∟ Spinocerebellar Degenerations ∟ Spinocerebellar Ataxias 3 coordinate concepts 2 subordinate concepts ∟ Ataxia Telangiectasia \| ∟ Machado-Joseph Disease ∟ Friedreich Ataxia \| ∟ Myoclonic Cerebellar Dyssynergia \| ∟ Olivopontocerebellar Atrophies Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurologic Manifestations ∟ Dyskinesias ∟ Ataxia ∟ Cerebellar Ataxia ∟ Spinocerebellar Ataxias 3 coordinate concepts 2 subordinate concepts ∟ Ataxia Telangiectasia \| ∟ Machado-Joseph Disease ∟ Friedreich Ataxia \| ∟ Myoclonic Cerebellar Dyssynergia \| ∟ Olivopontocerebellar Atrophies Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Signs and Symptoms ∟ Neurologic Manifestations ∟ Dyskinesias ∟ Ataxia ∟ Cerebellar Ataxia ∟ Spinocerebellar Ataxias 3 coordinate concepts 2 subordinate concepts ∟ Ataxia Telangiectasia \| ∟ Machado-Joseph Disease ∟ Friedreich Ataxia \| ∟ Myoclonic Cerebellar Dyssynergia \| ∟ Olivopontocerebellar Atrophies X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Heredodegenerative Disorders, Nervous System ∟ Spinocerebellar Degenerations ∟ Spinocerebellar Ataxias Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Cerebellar Diseases ∟ Cerebellar Ataxia ∟ Spinocerebellar Ataxias Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Cerebellar Diseases ∟ Spinocerebellar Degenerations ∟ Spinocerebellar Ataxias Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Spinal Cord Diseases ∟ Spinocerebellar Degenerations ∟ Spinocerebellar Ataxias Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurodegenerative Diseases ∟ Heredodegenerative Disorders, Nervous System ∟ Spinocerebellar Degenerations ∟ Spinocerebellar Ataxias Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurologic Manifestations ∟ Dyskinesias ∟ Ataxia ∟ Cerebellar Ataxia ∟ Spinocerebellar Ataxias Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Signs and Symptoms ∟ Neurologic Manifestations ∟ Dyskinesias ∟ Ataxia ∟ Cerebellar Ataxia ∟ Spinocerebellar Ataxias Spinocerebellar Degenerations > Heredodegenerative Disorders, Nervous System > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Cerebellar Ataxia > Cerebellar Diseases > Brain Diseases > Central Nervous System Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Spinocerebellar Degenerations > Cerebellar Diseases > Brain Diseases > Central Nervous System Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Spinocerebellar Degenerations > Spinal Cord Diseases > Central Nervous System Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Spinocerebellar Degenerations > Heredodegenerative Disorders, Nervous System > Neurodegenerative Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Cerebellar Ataxia > Ataxia > Dyskinesias > Neurologic Manifestations > Nervous System Diseases > Medical Subject Headings (MeSH) Cerebellar Ataxia > Ataxia > Dyskinesias > Neurologic Manifestations > Signs and Symptoms > Pathological Conditions, Signs and Symptoms > Medical Subject Headings (MeSH) X
Narrower terms:	Ataxia Telangiectasia \| Machado-Joseph Disease X
Annotation:	SPINOCEREBELLAR ATAXIA TYPE 3 see MACHADO-JOSEPH DISEASE is available X
History note:	Ataxia/genetics (1965-1999) \| Cerebellar Diseases (1966-1999) \| Spinal Cord Diseases (1966-1999) \| Spinocerebellar Degenerations (1987-1999)X
historyNote*:	2000; use SPINOCEREBELLAR DEGENERATION 1987-1999 X
publicMeSHNote*:	2000; see SPINOCEREBELLAR DEGENERATION 1987-1999 X
Scope note:	A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43) X
activeMeSHYear*:	2006 \| 2007X
dateCreated*:	1999-11-08X
dateEstablished*:	2000-01-01X
dateRevised*:	2005-06-30X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	KEVX
Type:	Concept X
Coordinate terms:	Friedreich Ataxia \| Myoclonic Cerebellar Dyssynergia \| Olivopontocerebellar Atrophies X
URI:	X
Labels and equivalent concepts:	Spinoserebellaariset ataksiat (fi) Spinoserebellaarinen ataksia (fi, replaced) Spinoserebellaariset atrofiat (fi, replaced) Spinoserebellaarinen atrofia (fi, replaced) Spinocerebellära ataxier (sv) Type 6 Spinocerebellar Ataxia (en, replaced) Type 5 Spinocerebellar Ataxia (en, replaced) Type 4 Spinocerebellar Ataxia (en, replaced) Type 7 Spinocerebellar Ataxia (en, replaced) Type 2 Spinocerebellar Ataxia (en, replaced) Type 1 Spinocerebellar Ataxia (en, replaced) Spinocerebellar Ataxia-4 (en, replaced) Spinocerebellar Ataxia-2 (en, replaced) Spinocerebellar Ataxia-1 (en, replaced) Spinocerebellar Ataxia-5 (en, replaced) Spinocerebellar Ataxia-6 (en, replaced) Spinocerebellar Atrophies (en, replaced) Spinocerebellar Ataxias, Dominantly-Inherited (en, replaced) Spinocerebellar Ataxia-7 (en, replaced) Dominantly-Inherited Spinocerebellar Ataxias (en, replaced) Ataxia spinocerebellaris (la-FI, replaced) X
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