Spinocerebellar Degenerations

"Spinocerebellar Degenerations" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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.

Descriptor ID	D013132
MeSH Number(s)	C10.228.140.252.700 C10.228.854.787 C10.574.500.825 C16.320.400.780
Concept/Terms	Spinocerebellar Degenerations Spinocerebellar Degenerations Degeneration, Spinocerebellar Degenerations, Spinocerebellar Spinocerebellar Diseases Spinocerebellar Disease Spinocerebellar Degeneration Spino Cerebellar Degenerations Degeneration, Spino Cerebellar Degenerations, Spino Cerebellar Spino Cerebellar Degeneration Spino-Cerebellar Degenerations Degeneration, Spino-Cerebellar Spino-Cerebellar Degeneration Cerebellar Ataxia, Early Onset Cerebellar Ataxia, Early Onset Early Onset Cerebellar Ataxia Marinesco-Sjogren Syndrome Marinesco-Sjogren Syndrome Marinesco Sjogren Syndrome Syndrome, Marinesco-Sjogren Hereditary Oligophrenic Cerebello-Lental Degeneration Hereditary Oligophrenic Cerebello Lental Degeneration Marinesco-Sjögren Syndrome Marinesco Sjögren Syndrome Syndrome, Marinesco-Sjögren Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism Hypogonadism, Marinesco-Sjogren Syndrome-Hypergonadotrophic Marinesco Sjogren Syndrome Hypergonadotrophic Hypogonadism Syndrome-Hypergonadotrophic Hypogonadism, Marinesco-Sjogren Marinesco-Sjogren Syndrome-Myopathy Marinesco Sjogren Syndrome Myopathy Syndrome-Myopathy, Marinesco-Sjogren Marinesco-Sjogren-Garland Syndrome Marinesco Sjogren Garland Syndrome Syndrome, Marinesco-Sjogren-Garland Garland-Moorhouse Syndrome Garland Moorhouse Syndrome Syndrome, Garland-Moorhouse Marinesco-Garland Syndrome Marinesco Garland Syndrome Syndrome, Marinesco-Garland Cerebellar Degenerations, Primary Cerebellar Degenerations, Primary Cerebellar Degeneration, Primary Degeneration, Primary Cerebellar Degenerations, Primary Cerebellar Primary Cerebellar Degeneration Primary Cerebellar Degenerations Corticostriatal-Spinal Degeneration Corticostriatal-Spinal Degeneration Corticostriatal Spinal Degeneration Corticostriatal-Spinal Degenerations Degeneration, Corticostriatal-Spinal Degenerations, Corticostriatal-Spinal Marie Cerebellar Ataxia Marie Cerebellar Ataxia Cerebellar Ataxia, Marie Marie's Cerebellar Ataxia Cerebellar Ataxia, Marie's Ataxias, Hereditary Ataxias, Hereditary Ataxia, Hereditary Hereditary Ataxia Hereditary Ataxias Hereditary Spinocerebellar Degenerations Degeneration, Hereditary Spinocerebellar Degenerations, Hereditary Spinocerebellar Hereditary Spinocerebellar Degeneration Spinocerebellar Degeneration, Hereditary Spinocerebellar Degenerations, Hereditary Inherited Spinocerebellar Degenerations Degeneration, Inherited Spinocerebellar Degenerations, Inherited Spinocerebellar Inherited Spinocerebellar Degeneration Spinocerebellar Degeneration, Inherited Spinocerebellar Degenerations, Inherited Familial Spinocerebellar Degenerations Degeneration, Familial Spinocerebellar Degenerations, Familial Spinocerebellar Familial Spinocerebellar Degeneration Spinocerebellar Degeneration, Familial Spinocerebellar Degenerations, Familial Cerebellar Ataxia, Late Onset Cerebellar Ataxia, Late Onset Late Onset Cerebellar Ataxia

Below are MeSH descriptors whose meaning is more general than "Spinocerebellar Degenerations".

Diseases [C]
Nervous System Diseases [C10]
Central Nervous System Diseases [C10.228]
Brain Diseases [C10.228.140]
Cerebellar Diseases [C10.228.140.252]
Spinocerebellar Degenerations [C10.228.140.252.700]
Spinal Cord Diseases [C10.228.854]
Spinocerebellar Degenerations [C10.228.854.787]
Neurodegenerative Diseases [C10.574]
Heredodegenerative Disorders, Nervous System [C10.574.500]
Spinocerebellar Degenerations [C10.574.500.825]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Heredodegenerative Disorders, Nervous System [C16.320.400]
Spinocerebellar Degenerations [C16.320.400.780]

Below are MeSH descriptors whose meaning is related to "Spinocerebellar Degenerations".

Below are MeSH descriptors whose meaning is more specific than "Spinocerebellar Degenerations".

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