Details of Disease | DrugMAP

General Information of Disease (ID: DIS9XHJR)

Disease Name	Spastic paraplegia 88, autosomal dominant
Disease Hierarchy	DISGZQV1: Hereditary spastic paraplegia DIS9XHJR: Spastic paraplegia 88, autosomal dominant
Disease Identifiers	MONDO ID MONDO_0859309 UMLS CUI C5774247 OMIM ID 620106 MedGen ID 1824020

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
KPNA3	OTLI3TM2	Strong	Autosomal dominant	[1]
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References

1	KPNA3 variation is associated with schizophrenia, major depression, opiate dependence and alcohol dependence. Dis Markers. 2012;33(4):163-70. doi: 10.3233/DMA-2012-0921.