autosomal recessive distal hereditary motor neuronopathy 7 (DOID:0081426)
Alliance: disease page
Alt IDs: OMIM:619216
Definition: An autosomal recessive distal hereditary motor neuronopathy characterized by onset of lower leg weakness in the first decade and that has_material_basis_in homozygous or compound heterozygous mutation in the VWA1 gene on chromosome 1p36.