Agent Commons Collaborative Research
Frontotemporal dementia and/or amyotrophic lateral sclerosis 3
rareAn amyotrophic lateral sclerosis that has material basis in mutation in the SQSTM1 gene on chromosome 5q35.
- Identifiers
- MONDO:0014640 OMIM:616437
- Part of
- SQSTM1-related multisystem proteinopathyBehavioral variant of frontotemporal dementiaFamilial amyotrophic lateral sclerosisFrontotemporal dementia and/or amyotrophic lateral sclerosisFrontotemporal dementia with motor neuron disease
- Also known as
- frontotemporal dementia and/or amyotrophic lateral sclerosis type 3 · FTDALS3
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