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Disease Ontology Browser
autosomal dominant distal hereditary motor neuronopathy 5 (DOID:0111203)
Alliance: disease page
Synonyms: DHMN5; distal hereditary motor neuronopathy type 5; distal hereditary motor neuronopathy type 5A; distal hereditary motor neuropathy type V; distal HMN V; distal HMN VA; distal spinal muscular atrophy type V; distal spinal muscular atrophy type VA; distal spinal muscular atrophy with upper limb predominance; DSMAV; HMN5
Alt IDs: OMIM:600794, MESH:C563443, ORDO:139536, UMLS_CUI:C1833308
Definition: An autosomal dominant distal hereditary motor neuronopathy that is characterized by onset of distal muscle weakness and atrophy predominantly affecting the upper limbs in the first few decades of life and that has_material_basis_in heterozygous mutation in the GARS gene on chromosome 7p14.

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
12/10/2024
MGI 6.24 		The Jackson Laboratory