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Metadata
ID	DOID:0081380
Name	amyotrophic lateral sclerosis type 26
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. https://pubmed.ncbi.nlm.nih.gov/28817800/
Xrefs	MIM:619133
Parent Relationships	is_a autosomal dominant disease is_a amyotrophic lateral sclerosis
Subclass Logical Relationships	existence starts during some Adult onset has material basis in some autosomal dominant inheritance