Term Name:	autosomal recessive distal hereditary motor neuronopathy 10
Synonyms:
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.
Ontology:	Human Disease [DOID:0081429]   ( DOID:0081429 )