Details of Disease | DrugMAP

General Information of Disease (ID: DIS17A1W)

Disease Name	Hereditary cerebellar ataxia
Synonyms	hereditary cerebellar ataxia; cerebellar hereditary ataxia
Definition	Cerebellar ataxia that is transmitted from parent to child.
Disease Hierarchy	DIS6JNI3: Hereditary ataxia DIS9IRAV: Cerebellar ataxia DIS17A1W: Hereditary cerebellar ataxia
Disease Identifiers	MONDO ID MONDO_0100310 MESH ID D013132 UMLS CUI C0270749 MedGen ID 78726 SNOMED CT ID 46808003

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
PRKCG	TTRFOXJ	Strong	Genetic Variation	[1]
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This Disease Is Related to 2 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
BEAN1	OT0WLH27	Strong	Genetic Variation	[2]
TK2	OTS1V4XB	Strong	Genetic Variation	[2]
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References

1	Spinocerebellar ataxia type 14.Handb Clin Neurol. 2012;103:555-9. doi: 10.1016/B978-0-444-51892-7.00036-X.
2	SCA31 is rare in the Chinese population on Taiwan.Neurobiol Aging. 2012 Feb;33(2):426.e23-4. doi: 10.1016/j.neurobiolaging.2010.10.012. Epub 2010 Dec 15.