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Cell Culture Ontology
Last uploaded:
July 23, 2014
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Preferred Name | obsolete_spinocerebellar ataxia | |
Synonyms |
Spinocerebellar ataxia (disorder) Spinocerebellar Atrophy Spinocerebellar Ataxias Dominantly-Inherited Spinocerebellar Ataxia |
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Definitions |
A group of dominantly inherited, predominatly 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 (MeSH). |
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ID |
http://www.ebi.ac.uk/efo/EFO_0002624 |
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Obsolete |
true |
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database_cross_reference |
OMIM:164400 NIFSTD:birnlex_12648 DOID:1441
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definition |
A group of dominantly inherited, predominatly 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 (MeSH).
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deprecated |
true
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has_exact_synonym |
Spinocerebellar ataxia (disorder) Spinocerebellar Atrophy Spinocerebellar Ataxias Dominantly-Inherited Spinocerebellar Ataxia
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label |
obsolete_spinocerebellar ataxia
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obsoleted_in_version |
2.32
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organizational_class |
true
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preferred label |
obsolete_spinocerebellar ataxia
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prefixIRI |
efo:EFO_0002624
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prefLabel |
obsolete_spinocerebellar ataxia
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reason_for_obsolescence |
Reorganised according to Orphanet hierarchy
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term editor |
Tomasz Adamusiak Ele Holloway
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subClassOf |
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Delete | Subject | Author | Type | Created |
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Mapping To | Ontology | Source |
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http://www.ebi.ac.uk/efo/EFO_0002624 | CLO | SAME_URI |
http://www.ebi.ac.uk/efo/EFO_0002624 | EFO | SAME_URI |
http://www.ebi.ac.uk/efo/EFO_0002624 | EFO | LOOM |