Term Name:	autosomal recessive distal hereditary motor neuronopathy 3
Synonyms:	autosomal recessive distal spinal muscular atrophy type 3, dHMN3, dHMN3 and dHMN4, dHMN4, distal hereditary motor neuropathy type 3, distal hereditary motor neuropathy type 3 and type 4, distal hereditary motor neuropathy type 4, distal spinal muscular atrophy type 3, dSMA3
Definition:	An autosomal recessive distal hereditary motor neuronopathy characterized by juvenile onset of distal muscle weakness and wasting with variable severity that has_material_basis_in homozygous mutation in a 2.6-cM region of chromosome 11q13.3.
Ontology:	Human Disease [DOID:0111211]   ( DOID:0111211 )