Details of Disease | DrugMAP

General Information of Disease (ID: DIS2OBPK)

Disease Name	Neuronopathy, distal hereditary motor, type 9
Synonyms	HMN9; neuropathy, distal hereditary motor, type 9; neuronopathy, distal hereditary motor, type IX
Disease Hierarchy	DIS4M3WN: Neuronopathy, distal hereditary motor, autosomal dominant DIS2OBPK: Neuronopathy, distal hereditary motor, type 9
Disease Identifiers	MONDO ID MONDO_0060585 UMLS CUI C4540265 OMIM ID 617721 MedGen ID 1617571

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
WARS1	OTWKTPGC	Strong	Autosomal dominant	[1]
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This Disease Is Related to 2 DME Molecule(s)

Gene Name	DME ID	Evidence Level	Mode of Inheritance	REF
WARS1	DEPVE0M	Strong	Autosomal dominant	[1]
WARS1	DEPVE0M	Strong	Genetic Variation	[1]
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References

1	A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy. Brain. 2017 May 1;140(5):1252-1266. doi: 10.1093/brain/awx058.