Search Ontology:
Human Disease

frontotemporal dementia and/or amyotrophic lateral sclerosis 2

Term ID
DOID:0060214
Synonyms
  • FTDALS2
Definition
An amyotrophic lateral sclerosis that has_material_basis_in mutation in the CHCHD10 gene on chromosome 22. It is characterized by adult onset of either frontotemporal dementia and/or amyotrophic lateral sclerosis. (2)
References
Ontology
Human Disease   ( DOID:0060214 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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