amyotrophic lateral sclerosis type 26 (DOID:0081380)
Alliance: disease page
Alt IDs: OMIM:619133
Definition: An amyotrophic lateral sclerosis that is characterized by adult onset of upper and low motor neuron disease causing bulbar dysfunction and limb weakness and that has_material_basis_in heterozygous mutation in the TIA1 gene on chromosome 2p13.