amyotrophic lateral sclerosis type 26

Term ID

DOID:0081380

Synonyms

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/

References

• OMIM:619133

Ontology

Human Disease   ( DOID:0081380 )