# FTDALS2

> 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

**Wikidata**: [Q18553731](https://www.wikidata.org/wiki/Q18553731)  
**Source**: https://4ort.xyz/entity/ftdals2


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)