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Descriptor English: Spinocerebellar Degenerations
Descriptor Spanish: Degeneraciones Espinocerebelosas
Descriptor degeneraciones espinocerebelosas
Entry term(s) ataxia cerebelosa de Marie
ataxia cerebelosa de comienzo tardío
ataxia cerebelosa de comienzo temprano
ataxias hereditarias
degeneraciones cerebelosas primarias
degeneración corticoestriatal-espinal
degeneración espinocerebelosa
síndrome de Marinesco-Sjogren
Scope note: Grupo heterogéneo de síndromes degenerativos que se caracterizan por disfunción cerebelosa progresiva, tanto aislada como combinada con otras manifestaciones neurológicas. Hay subtipos esporádicos y hereditarios. Los patrones hereditarios pueden ser autosómicos dominantes, autosómicos recesivos y ligados al cromosoma X.
Descriptor Portuguese: Degenerações Espinocerebelares
Descriptor French: Dégénérescences spinocérébelleuses
Entry term(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
Tree number(s): C10.228.140.252.700
C10.228.854.787
C10.574.500.825
C16.320.400.780
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D013132
Scope note: 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.
Allowable Qualifiers: 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
Previous Indexing: Cerebellar Ataxia (1968-1986)
Cerebellar Diseases (1966-1986)
Spinal Cord Diseases (1966-1986)
Public MeSH Note: 2000; see SPINOCEREBELLAR DEGENERATION 1989-1999, see SPINOCEREBELLAR DEGENERATIONS 1987-1988
History Note: 2000(1987)
DeCS ID: 24409
Unique ID: D013132
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1987/01/01
Date of Entry: 1986/03/31
Revision Date: 2013/07/08
Spinocerebellar Degenerations - Preferred
Concept UI M0020336
Scope note 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.
Preferred term Spinocerebellar Degenerations
Entry term(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
Cerebellar Ataxia, Early Onset - Narrower
Concept UI M0336205
Preferred term Cerebellar Ataxia, Early Onset
Entry term(s) Early Onset Cerebellar Ataxia
Marinesco-Sjogren Syndrome - Narrower
Concept UI M0020335
Preferred term Marinesco-Sjogren Syndrome
Entry term(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
Cerebellar Degenerations, Primary - Narrower
Concept UI M0336207
Preferred term Cerebellar Degenerations, Primary
Entry term(s) Cerebellar Degeneration, Primary
Degeneration, Primary Cerebellar
Degenerations, Primary Cerebellar
Primary Cerebellar Degeneration
Primary Cerebellar Degenerations
Corticostriatal-Spinal Degeneration - Narrower
Concept UI M0336208
Preferred term Corticostriatal-Spinal Degeneration
Entry term(s) Corticostriatal Spinal Degeneration
Corticostriatal-Spinal Degenerations
Degeneration, Corticostriatal-Spinal
Degenerations, Corticostriatal-Spinal
Marie Cerebellar Ataxia - Narrower
Concept UI M0336209
Preferred term Marie Cerebellar Ataxia
Entry term(s) Cerebellar Ataxia, Marie
Cerebellar Ataxia, Marie's
Marie's Cerebellar Ataxia
Ataxias, Hereditary - Broader
Concept UI M0020334
Preferred term Ataxias, Hereditary
Entry term(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
Cerebellar Ataxia, Late Onset - Narrower
Concept UI M0336206
Preferred term Cerebellar Ataxia, Late Onset
Entry term(s) Late Onset Cerebellar Ataxia



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