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Diseases

Spinocerebellar Degeneration

spinocerebellar degeneration

Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

Grouped by core information, identifiers, and descriptions.

Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name
Spinocerebellar Degeneration
Standard Disease Name
spinocerebellar degeneration
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D013132
OMIM ID
MTHU009343
UMLS ID
C0037952
HPO ID
No data

Description and Extensions

Description
MSH2017_2016_08_12: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.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
03
CACNA1A
calcium voltage-gated channel subunit alpha1 A
calcium voltage-gated channel subunit alpha1 A
04
CRH
corticotropin releasing hormone
corticotropin releasing hormone