autosomal recessive distal hereditary motor neuronopathy 10 (DOID:0081429)
Alliance: disease page
Alt IDs: OMIM:620542
Definition: An autosomal recessive distal hereditary motor neuronopathy characterized by distal muscle weakness and atrophy predominantly affecting the lower limbs and resulting in gait abnormalities and that has_material_basis_in homozygous or compound heterozygous mutation in the VRK1 gene on chromosome 14q32.