Term Name:	autosomal dominant distal hereditary motor neuronopathy 6
Synonyms:	distal hereditary motor neuronopathy type 2D, distal hereditary motor neuropathy type IID, distal spinal muscular atrophy with calf predominance, HMN IID, HMN2D
Definition:	A distal hereditary motor neuropathy that has_material_basis_in heterozygous mutation in the FBXO38 gene on 5q32.
Ontology:	Human Disease [DOID:0111210]   ( DOID:0111210 )