Term Name:	amyotrophic lateral sclerosis type 4
Synonyms:	ALS4, amyotrophic lateral sclerosis 4, amyotrophic lateral sclerosis 4, juvenile, dHMN with upper motor neuron signs, distal hereditary motor neuropathy with pyramidal features, distal hereditary motor neuropathy with upper motor neuron signs
Definition:	An amyotrophic lateral sclerosis with juvenile onset that has_material_basis_in mutation in the SETX gene on chromosome 9.
Ontology:	Human Disease [DOID:0060196]   ( DOID:0060196 )