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Disease Ontology Browser
frontotemporal dementia and/or amyotrophic lateral sclerosis 2 (DOID:0060214)
Alliance: disease page
Synonyms: FTDALS2
Alt IDs: OMIM:615911
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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory