Search Ontology:
Human Disease

amyotrophic lateral sclerosis type 23

Term ID
DOID:0080225
Synonyms
Definition
An amyotrophic lateral sclerosis that has_material_basis_in heterozygous mutation in the ANXA11 gene on chromosome 10q22. https://pubmed.ncbi.nlm.nih.gov/28469040/
References
Ontology
Human Disease   ( DOID:0080225 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models