Term Name:	hereditary spastic paraplegia 39
Synonyms:	autosomal recessive spastic paraplegia 39, autosomal recessive spastic paraplegia type 39, NTE-related motor neuron disorder, NTEMND, spastic paraplegia due to neuropathy target esterase mutation, spastic paraplegia due to NTE mutation, SPG39
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the PNPLA6 gene on chromosome 19p13.
Ontology:	Human Disease [DOID:0110790]   ( DOID:0110790 )