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 )
- is a type of
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