Details of Disease | DrugMAP

General Information of Disease (ID: DISWHXC7)

Disease Name	Autosomal recessive spastic paraplegia type 66
Synonyms	SPG66
Disease Hierarchy	DIS9KXQY: Complex hereditary spastic paraplegia DISWHXC7: Autosomal recessive spastic paraplegia type 66
Disease Identifiers	MONDO ID MONDO_0018418 UMLS CUI C5190590 MedGen ID 1675102 Orphanet ID 401815 SNOMED CT ID 782747000

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
ARSI	OTIANNWW	Supportive	Autosomal recessive	[1]
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References

1	Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders. Science. 2014 Jan 31;343(6170):506-511. doi: 10.1126/science.1247363.