Term Name:	autosomal dominant distal hereditary motor neuronopathy 10
Synonyms:
Definition:	An autosomal dominant distal hereditary motor neuronopathy that is characterized clinically by length-dependent motor neuropathy primarily affecting the lower limbs and that has_material_basis_in heterozygous mutation in the EMILIN1 gene on chromosome 2p23.
Ontology:	Human Disease [DOID:0081399]   ( DOID:0081399 )