familial amyotrophic lateral sclerosis
MONDO:0005144Mondo
Findings
No curated finding names familial amyotrophic lateral sclerosis yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An instance of amyotrophic lateral sclerosis that is caused by an inherited modification of the individual's genome.
Definition from the Mondo Disease Ontology (MONDO:0005144), read 2026-09-29. CC BY 4.0.
Where it sits
- Narrower terms (29)
- amyotrophic lateral sclerosis 26 with or without frontotemporal dementia
- amyotrophic lateral sclerosis 27, juvenile
- amyotrophic lateral sclerosis 28
- amyotrophic lateral sclerosis type 1
- amyotrophic lateral sclerosis type 10
- amyotrophic lateral sclerosis type 11
- amyotrophic lateral sclerosis type 12
- amyotrophic lateral sclerosis type 15
- amyotrophic lateral sclerosis type 18
- amyotrophic lateral sclerosis type 19
- amyotrophic lateral sclerosis type 20
- amyotrophic lateral sclerosis type 21
- amyotrophic lateral sclerosis type 22
- amyotrophic lateral sclerosis type 23
- amyotrophic lateral sclerosis type 3
- amyotrophic lateral sclerosis type 4
- amyotrophic lateral sclerosis type 6
- amyotrophic lateral sclerosis type 7
- amyotrophic lateral sclerosis type 8
- amyotrophic lateral sclerosis type 9
- frontotemporal dementia and/or amyotrophic lateral sclerosis 1
- frontotemporal dementia and/or amyotrophic lateral sclerosis 2
- frontotemporal dementia and/or amyotrophic lateral sclerosis 3
- frontotemporal dementia and/or amyotrophic lateral sclerosis 4
- frontotemporal dementia and/or amyotrophic lateral sclerosis 5
- frontotemporal dementia and/or amyotrophic lateral sclerosis 6
- frontotemporal dementia and/or amyotrophic lateral sclerosis 7
- frontotemporal dementia and/or amyotrophic lateral sclerosis 8
- juvenile amyotrophic lateral sclerosis
Other names
1 name
Resolves to: familial amyotrophic lateral sclerosis
- Also called
- hereditary amyotrophic lateral sclerosis