Term Name: autosomal recessive distal hereditary motor neuronopathy 7
Synonyms:
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.
Ontology: Human Disease [DOID:0081426]   ( DOID:0081426 )

Relationships
is a type of: autosomal recessive distal hereditary motor neuronopathy