autosomal dominant distal hereditary motor neuronopathy 6 (DOID:0111210)
Alliance: disease page
Synonyms: distal hereditary motor neuronopathy type 2D; distal hereditary motor neuropathy type IID; distal spinal muscular atrophy with calf predominance; HMN2D; HMN IID
Alt IDs: OMIM:615575
Definition: A distal hereditary motor neuropathy that has_material_basis_in heterozygous mutation in the FBXO38 gene on 5q32.