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Disease Ontology Browser
autosomal dominant distal hereditary motor neuronopathy (DOID:0111198)
Alliance: disease page
Synonyms: autosomal dominant dHMN; autosomal dominant distal hereditary motor neuropathy; autosomal dominant distal spinal muscular atrophy
Alt IDs: OMIM:PS182960, ORDO:140465
Definition: A spinal muscular atrophy that is characterized by progressive distal motor weakness and muscular atrophy of the peripheral nervous system without sensory impairment, that is caused by anterior horn cell degeneration, and that has_material_basis_in autosomal dominant inheritance.

Disease References using Mouse Models (1)
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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11/12/2024
MGI 6.24 		The Jackson Laboratory