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DOID:0111203 - distal hereditary motor neuronopathy type 5
Disease Ontology Definition:An autosomal dominant distal hereditary motor neuronopathy characterized by muscle weakness and wasting, predominantly confined to the hands, and often exclusively involve thenar and/or interosseus dorsalis I eminences.
Synonyms: DHMN5, DSMAV, HMN5, distal HMN V, distal hereditary motor neuropathy type V, distal spinal muscular atrophy type V, distal spinal muscular atrophy with upper limb predominance,
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee