Search Ontology:
Human Disease

amyotrophic lateral sclerosis type 13

Term ID
DOID:0060204
Synonyms
  • ALS13
  • amyotrophic lateral sclerosis 13
Definition
An amyotrophic lateral sclerosis where a mutation that has_material_basis_in the ATXN2 gene on chromosome 12 contributes to suscepitbility. (2)
References
Ontology
Human Disease   ( DOID:0060204 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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