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Disease Ontology Browser
autosomal dominant distal hereditary motor neuronopathy 9 (DOID:0111212)
Alliance: disease page
Synonyms: DHMN9; distal hereditary motor neuronopathy type 9; distal hereditary motor neuropathy type IX; HMN9
Alt IDs: OMIM:617721
Definition: An autosomal domiant distal hereditary motor neuronopathy that is characterized by juvenile onset of slowly progressive distal muscle weakness and atrophy affecting both the lower and upper limbs that has_material_basis_in heterozygous mutation in the WARS gene on 14q32.2.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory