Search Ontology:
Human Disease

amyotrophic lateral sclerosis type 18

Term ID
DOID:0060209
Synonyms
  • ALS18
  • amyotrophic lateral sclerosis 18
Definition
An amyotrophic lateral sclerosis that has_material_basis_in mutation in the PFN1 gene on chromosome 17. (2)
References
Ontology
Human Disease   ( DOID:0060209 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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