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DOID:0111206 - autosomal dominant distal hereditary motor neuronopathy 2
Disease Ontology Definition:An autosomal dominant distal hereditary motor neuronopathy that is characterized by onset of slowly progressive distal limb weakness and atrophy between the second and fifth decades of life.
Synonyms: autosomal dominant adult spinal muscular atrophy IIA, distal hereditary motor neuronopathy type 2, distal hereditary motor neuronopathy type 2A, distal hereditary motor neuropathy type II, distal hereditary motor neuropathy type IIA, HMN2, HMN2A, HMN II, HMN IIA, spinal Charcot-Marie-Tooth disease IIA
Xenbase Genes : hspb1, hspb8
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee