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Human Disease

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
Ontology
Human Disease   ( DOID:0081380 )
Relationships
is a type of
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Genes Involved
Zebrafish Models