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| Descritor em português: | Degenerações Espinocerebelares | ||||||
| Descritor em inglês: | Spinocerebellar Degenerations | ||||||
| Descritor em espanhol: |
Degeneraciones Espinocerebelosas
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| Descritor em francês: | Dégénérescences spinocérébelleuses | ||||||
| Termo(s) alternativo(s): |
Ataxia, Hereditary Ataxias, Hereditary Cerebellar Ataxia, Early Onset Cerebellar Ataxia, Late Onset Cerebellar Ataxia, Marie Cerebellar Ataxia, Marie's Cerebellar Degeneration, Primary Cerebellar Degenerations, Primary Corticostriatal Spinal Degeneration Corticostriatal-Spinal Degeneration Corticostriatal-Spinal Degenerations Degeneration, Corticostriatal-Spinal Degeneration, Familial Spinocerebellar Degeneration, Hereditary Spinocerebellar Degeneration, Inherited Spinocerebellar Degeneration, Primary Cerebellar Degeneration, Spino Cerebellar Degeneration, Spino-Cerebellar Degeneration, Spinocerebellar Degenerations, Corticostriatal-Spinal Degenerations, Familial Spinocerebellar Degenerations, Hereditary Spinocerebellar Degenerations, Inherited Spinocerebellar Degenerations, Primary Cerebellar Degenerations, Spino Cerebellar Degenerations, Spinocerebellar Early Onset Cerebellar Ataxia Familial Spinocerebellar Degeneration Familial Spinocerebellar Degenerations Garland Moorhouse Syndrome Garland-Moorhouse Syndrome Hereditary Ataxia Hereditary Ataxias Hereditary Oligophrenic Cerebello Lental Degeneration Hereditary Oligophrenic Cerebello-Lental Degeneration Hereditary Spinocerebellar Degeneration Hereditary Spinocerebellar Degenerations Hypogonadism, Marinesco-Sjogren Syndrome-Hypergonadotrophic Inherited Spinocerebellar Degeneration Inherited Spinocerebellar Degenerations Late Onset Cerebellar Ataxia Marie Cerebellar Ataxia Marie's Cerebellar Ataxia Marinesco Garland Syndrome Marinesco Sjogren Garland Syndrome Marinesco Sjogren Syndrome Marinesco Sjogren Syndrome Hypergonadotrophic Hypogonadism Marinesco Sjogren Syndrome Myopathy Marinesco Sjögren Syndrome Marinesco-Garland Syndrome Marinesco-Sjogren Syndrome Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism Marinesco-Sjogren Syndrome-Myopathy Marinesco-Sjogren-Garland Syndrome Marinesco-Sjögren Syndrome Primary Cerebellar Degeneration Primary Cerebellar Degenerations Spino Cerebellar Degeneration Spino Cerebellar Degenerations Spino-Cerebellar Degeneration Spino-Cerebellar Degenerations Spinocerebellar Degeneration Spinocerebellar Degeneration, Familial Spinocerebellar Degeneration, Hereditary Spinocerebellar Degeneration, Inherited Spinocerebellar Degenerations, Familial Spinocerebellar Degenerations, Hereditary Spinocerebellar Degenerations, Inherited Spinocerebellar Disease Spinocerebellar Diseases Syndrome, Garland-Moorhouse Syndrome, Marinesco-Garland Syndrome, Marinesco-Sjogren Syndrome, Marinesco-Sjogren-Garland Syndrome, Marinesco-Sjögren Syndrome-Hypergonadotrophic Hypogonadism, Marinesco-Sjogren Syndrome-Myopathy, Marinesco-Sjogren |
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| Código(s) hierárquico(s): |
C10.228.140.252.700 C10.228.854.787 C10.574.500.825 C16.320.400.780 |
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| Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D013132 | ||||||
| Nota de escopo: | A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked. |
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| Qualificadores permitidos: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Indexação Anterior: |
Cerebellar Ataxia (1968-1986) Cerebellar Diseases (1966-1986) Spinal Cord Diseases (1966-1986) |
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| Nota MeSH pública: | 2000; see SPINOCEREBELLAR DEGENERATION 1989-1999, see SPINOCEREBELLAR DEGENERATIONS 1987-1988 |
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| Nota histórica: | 2000(1987) |
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| Identificador DeCS: | 24409 | ||||||
| ID do descritor: | D013132 | ||||||
| Documentos indexados na Biblioteca Virtual em Saúde (BVS): | Clique aqui para acessar os documentos da BVS | ||||||
| Data de estabelecimento: | 01/01/1987 | ||||||
| Data de entrada: | 31/03/1986 | ||||||
| Data de revisão: | 08/07/2013 |
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Spinocerebellar Degenerations
- Conceito preferido
Cerebellar Ataxia, Early Onset
- Mais específico
Marinesco-Sjogren Syndrome
- Mais específico
Cerebellar Degenerations, Primary
- Mais específico
Corticostriatal-Spinal Degeneration
- Mais específico
Marie Cerebellar Ataxia
- Mais específico
Ataxias, Hereditary
- Mais amplo
Cerebellar Ataxia, Late Onset
- Mais específico
| Identificador do conceito |
M0020336 |
| Nota de escopo | A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked. |
| Termo preferido | Spinocerebellar Degenerations |
| Termo(s) alternativo(s) |
Degeneration, Spino Cerebellar Degeneration, Spino-Cerebellar Degeneration, Spinocerebellar Degenerations, Spino Cerebellar Degenerations, Spinocerebellar Spino Cerebellar Degeneration Spino Cerebellar Degenerations Spino-Cerebellar Degeneration Spino-Cerebellar Degenerations Spinocerebellar Degeneration Spinocerebellar Disease Spinocerebellar Diseases |
| Identificador do conceito |
M0336205 |
| Termo preferido | Cerebellar Ataxia, Early Onset |
| Termo(s) alternativo(s) |
Early Onset Cerebellar Ataxia |
| Identificador do conceito |
M0020335 |
| Termo preferido | Marinesco-Sjogren Syndrome |
| Termo(s) alternativo(s) |
Garland Moorhouse Syndrome Garland-Moorhouse Syndrome Hereditary Oligophrenic Cerebello Lental Degeneration Hereditary Oligophrenic Cerebello-Lental Degeneration Hypogonadism, Marinesco-Sjogren Syndrome-Hypergonadotrophic Marinesco Garland Syndrome Marinesco Sjogren Garland Syndrome Marinesco Sjogren Syndrome Marinesco Sjogren Syndrome Hypergonadotrophic Hypogonadism Marinesco Sjogren Syndrome Myopathy Marinesco Sjögren Syndrome Marinesco-Garland Syndrome Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism Marinesco-Sjogren Syndrome-Myopathy Marinesco-Sjogren-Garland Syndrome Marinesco-Sjögren Syndrome Syndrome, Garland-Moorhouse Syndrome, Marinesco-Garland Syndrome, Marinesco-Sjogren Syndrome, Marinesco-Sjogren-Garland Syndrome, Marinesco-Sjögren Syndrome-Hypergonadotrophic Hypogonadism, Marinesco-Sjogren Syndrome-Myopathy, Marinesco-Sjogren |
| Identificador do conceito |
M0336207 |
| Termo preferido | Cerebellar Degenerations, Primary |
| Termo(s) alternativo(s) |
Cerebellar Degeneration, Primary Degeneration, Primary Cerebellar Degenerations, Primary Cerebellar Primary Cerebellar Degeneration Primary Cerebellar Degenerations |
| Identificador do conceito |
M0336208 |
| Termo preferido | Corticostriatal-Spinal Degeneration |
| Termo(s) alternativo(s) |
Corticostriatal Spinal Degeneration Corticostriatal-Spinal Degenerations Degeneration, Corticostriatal-Spinal Degenerations, Corticostriatal-Spinal |
| Identificador do conceito |
M0336209 |
| Termo preferido | Marie Cerebellar Ataxia |
| Termo(s) alternativo(s) |
Cerebellar Ataxia, Marie Cerebellar Ataxia, Marie's Marie's Cerebellar Ataxia |
| Identificador do conceito |
M0020334 |
| Termo preferido | Ataxias, Hereditary |
| Termo(s) alternativo(s) |
Ataxia, Hereditary Degeneration, Familial Spinocerebellar Degeneration, Hereditary Spinocerebellar Degeneration, Inherited Spinocerebellar Degenerations, Familial Spinocerebellar Degenerations, Hereditary Spinocerebellar Degenerations, Inherited Spinocerebellar Familial Spinocerebellar Degeneration Familial Spinocerebellar Degenerations Hereditary Ataxia Hereditary Ataxias Hereditary Spinocerebellar Degeneration Hereditary Spinocerebellar Degenerations Inherited Spinocerebellar Degeneration Inherited Spinocerebellar Degenerations Spinocerebellar Degeneration, Familial Spinocerebellar Degeneration, Hereditary Spinocerebellar Degeneration, Inherited Spinocerebellar Degenerations, Familial Spinocerebellar Degenerations, Hereditary Spinocerebellar Degenerations, Inherited |
| Identificador do conceito |
M0336206 |
| Termo preferido | Cerebellar Ataxia, Late Onset |
| Termo(s) alternativo(s) |
Late Onset Cerebellar Ataxia |
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