Details of Disease | DrugMAP

General Information of Disease (ID: DISSU1KS)

Disease Name	Spastic paraplegia 85, autosomal recessive
Synonyms	SPG85; autosomal recessive spastic paraplegia type 85
Disease Hierarchy	DIS9KXQY: Complex hereditary spastic paraplegia DISSU1KS: Spastic paraplegia 85, autosomal recessive
Disease Identifiers	MONDO ID MONDO_0030512 UMLS CUI C5562053 OMIM ID 619686 MedGen ID 1794263

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
RNF170	OT2O6F4D	Strong	Autosomal recessive	[1]
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References

1	Age-dependent gait abnormalities in mice lacking the Rnf170 gene linked to human autosomal-dominant sensory ataxia. Hum Mol Genet. 2015 Dec 20;24(25):7196-206. doi: 10.1093/hmg/ddv417. Epub 2015 Oct 3.