Details of Disease | DrugMAP

General Information of Disease (ID: DISCI1YC)

Disease Name	Autosomal recessive spastic paraplegia type 69
Synonyms	SPG69
Disease Hierarchy	DIS9KXQY: Complex hereditary spastic paraplegia DISCI1YC: Autosomal recessive spastic paraplegia type 69
Disease Identifiers	MONDO ID MONDO_0018421 UMLS CUI C5190577 MedGen ID 1679277 Orphanet ID 401830 SNOMED CT ID 782725000

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
RAB3GAP2	OTQTE0GI	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.