obsolete distal hereditary motor neuronopathy type 7A (DOID:0111201)
Alliance: disease page
Definition: A distal hereditary motor neuropathy type 7 characterized by slowly progressive distal atrophy and weakness affecting first the upper limbs and later the lower limbs and vocal cord paresis that has_material_basis_in heterozygous mutation in SLC5A7 on 2q12.3.