Details of Disease | DrugMAP

General Information of Disease (ID: DISDMD53)

Disease Name	Spinocerebellar ataxia, autosomal recessive 25
Synonyms	SCAR25; autosomal recessive spinocerebellar ataxia 25; spinocerebellar ataxia, autosomal recessive 25
Disease Hierarchy	DISWBOUC: Autosomal recessive cerebellar ataxia DISDMD53: Spinocerebellar ataxia, autosomal recessive 25
Disease Identifiers	MONDO ID MONDO_0033115 UMLS CUI C4539808 OMIM ID 617584 MedGen ID 1618081

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
ATG5	OT4T5SMS	Limited	Autosomal recessive	[1]
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References

1	Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen). Genet Med. 2020 Feb;22(2):245-257. doi: 10.1038/s41436-019-0686-8. Epub 2019 Nov 6.