Term info
database cross reference
- OMIM:205100 (MONDO:equivalentTo)
- MESH:C565957 (MONDO:equivalentTo)
- DOID:0060194 (MONDO:equivalentTo)
- GARD:0009470 (MONDO:equivalentTo)
Subsets
gard_rare
definition
Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the ALS2 gene.
exactMatch
https://omim.org/entry/205100, http://identifiers.org/mesh/C565957, http://purl.obolibrary.org/obo/DOID_0060194
has exact synonym
ALS2, amyotrophic lateral sclerosis caused by mutation in ALS2, ALS2 amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 2, amyotrophic lateral sclerosis 2, juvenile
has related synonym
ALS, juvenile
id
MONDO:0008780
seeAlso
https://rarediseases.info.nih.gov/diseases/9470/amyotrophic-lateral-sclerosis-type-2