Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the UBQLN2 gene. [ MONDO : patterns/disease_series_by_gene ]

This is just here as a test because I lose it

Term information

database cross reference
definition
  • Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the UBQLN2 gene.
exactMatch
  • http://linkedlifedata.com/resource/umls/id/C3275459
  • https://omim.org/entry/300857
  • http://purl.obolibrary.org/obo/DOID_0060206
has exact synonym
  • UBQLN2 amyotrophic lateral sclerosis
  • amyotrophic lateral sclerosis 15
  • amyotrophic lateral sclerosis 15, with or without frontotemporal dementia
  • amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, X-linked dominant
  • amyotrophic lateral sclerosis caused by mutation in UBQLN2
  • amyotrophic lateral sclerosis type 15
  • ALS15
has related synonym
  • amyotrophic lateral sclerosis 15 with or without frontotemporal dementia
id
  • MONDO:0010459
seeAlso
  • https://github.com/monarch-initiative/mondo/issues/4521