Disease association ontology term - MONDO:0014395 - frontotemporal dementia and/or amyotrophic lateral sclerosis 2
Term summary
- ID
- MONDO:0014395
- Name
- frontotemporal dementia and/or amyotrophic lateral sclerosis 2
- Ontology or CV name
- Disease association
- 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.
