autosomal dominant distal hereditary motor neuronopathy 10 (DOID:0081399)
Alliance: disease page
Alt IDs: OMIM:620080
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.