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Diseases

Spinocerebellar Ataxia, Autosomal Recessive 1

spinocerebellar ataxia, autosomal recessive 1

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 Ataxia, Autosomal Recessive 1
Standard Disease Name
spinocerebellar ataxia, autosomal recessive 1
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
No data
OMIM ID
No data
UMLS ID
C1332961
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:A diffuse astrocytoma that arises from the cerebral hemispheres and occurs during childhood.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
04
ITPR1
inositol 1,4,5-trisphosphate receptor type 1
inositol 1,4,5-trisphosphate receptor type 1
07
POLG
DNA polymerase gamma, catalytic subunit
DNA polymerase gamma, catalytic subunit