Search Ontology:
Human Disease

amyotrophic lateral sclerosis type 20

Term ID
DOID:0060211
Synonyms
  • ALS20
  • amyotrophic lateral sclerosis 20
Definition
An amyotrophic lateral sclerosis with juvenile onset that has_material_basis_in mutation in the HNRNPA1 gene on chromosome 12. (2)
References
Ontology
Human Disease   ( DOID:0060211 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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