MeSH Browser

MeSH Heading: Spinocerebellar Degenerations
Tree Number(s): C10.228.140.252.700; C10.228.854.787; C10.574.500.825; C16.320.400.780
Unique ID: D013132
RDF Unique Identifier: http://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.
Entry Term(s): Ataxias, Hereditary; Cerebellar Ataxia, Early Onset; Cerebellar Ataxia, Late Onset; Cerebellar Degenerations, Primary; Corticostriatal-Spinal Degeneration; Early Onset Cerebellar Ataxia; Familial Spinocerebellar Degenerations; Garland-Moorhouse Syndrome; Hereditary Oligophrenic Cerebello-Lental Degeneration; Hereditary Spinocerebellar Degenerations; Inherited Spinocerebellar Degenerations; Late Onset Cerebellar Ataxia; Marie Cerebellar Ataxia; Marie's Cerebellar Ataxia; Marinesco-Garland Syndrome; Marinesco-Sjogren Syndrome; Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism; Marinesco-Sjogren Syndrome-Myopathy; Marinesco-Sjogren-Garland Syndrome; Marinesco-Sjögren Syndrome; Spino Cerebellar Degenerations; Spino-Cerebellar Degenerations; Spinocerebellar Degeneration; Spinocerebellar Diseases
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)
Date Established: 1987/01/01
Date of Entry: 1986/03/31
Revision Date: 2013/07/08

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

congenital (CN)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Nervous System Diseases [C10]
- Central Nervous System Diseases [C10.228]
  - Brain Diseases [C10.228.140]
    - Cerebellar Diseases [C10.228.140.252]

Nervous System Diseases [C10]
- Central Nervous System Diseases [C10.228]
  - Spinal Cord Diseases [C10.228.854]

Nervous System Diseases [C10]
- Neurodegenerative Diseases [C10.574]
  - Heredodegenerative Disorders, Nervous System [C10.574.500]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
  - Heredodegenerative Disorders, Nervous System [C16.320.400]

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.
Terms: Spinocerebellar Degenerations Preferred Term
Term UI T364820
Date11/03/1999
LexicalTag NON
ThesaurusID NLM (2000); Spino Cerebellar Degenerations
Term UI T038626
Date03/31/1986
LexicalTag NON
ThesaurusID UNK (19XX); Spino-Cerebellar Degenerations
Term UI T038627
Date03/31/1986
LexicalTag NON
ThesaurusID UNK (19XX); Spinocerebellar Degeneration
Term UI T038625
Date01/01/1999
LexicalTag NON
ThesaurusID NLM (1987); Spinocerebellar Diseases
Term UI T370689
Date11/03/1999
LexicalTag NON
ThesaurusID NLM (2000)

Marinesco-Sjogren Syndrome Narrower

Cerebellar Ataxia, Early Onset Narrower

Cerebellar Ataxia, Late Onset Narrower

Cerebellar Degenerations, Primary Narrower

Corticostriatal-Spinal Degeneration Narrower

Ataxias, Hereditary Broader

Marie Cerebellar Ataxia Narrower

Spinocerebellar Degenerations MeSH Descriptor Data 2024