autosomal recessive distal hereditary motor neuronopathy 9 (DOID:0081428)
Alliance: disease page
Alt IDs: OMIM:620402
Definition: An autosomal recessive distal hereditary motor neuronopathy characterized by juvenile onset of distal muscle weakness and atrophy, resulting in gait difficulties and that has_material_basis_in homozygous or compound heterozygous mutation in the COQ7 gene on chromosome 16p12.