Details of Disease | DrugMAP

General Information of Disease (ID: DISJ9W2D)

Disease Name	Autosomal dominant complex spastic paraplegia type 9B
Synonyms	AD-SPG9B
Disease Hierarchy	DIS3RP1V: Autosomal dominant spastic paraplegia type 9 DISJ9W2D: Autosomal dominant complex spastic paraplegia type 9B
Disease Identifiers	MONDO ID MONDO_0018644 UMLS CUI C5568979 MedGen ID 1800402 Orphanet ID 447757 SNOMED CT ID 1187466009

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
ALDH18A1	OT6W40XU	Supportive	Autosomal dominant	[1]
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References

1	Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia. Brain. 2015 Aug;138(Pt 8):2191-205. doi: 10.1093/brain/awv143. Epub 2015 May 29.