JSON

type 1 interferonopathy

Go to external page http://purl.obolibrary.org/obo/MONDO_0700264

Conditions in which increased type 1 interferon signaling leads to autoimmune and neurological disorders. These disorders are caused by variants in genes involved in nucleic acid metabolism, sensing, and the innate immune response. [ https://clinicalgenome.org/affiliation/40060/ https://clinicalgenome.org/affiliation/40107/ https://clinicalgenome.org/affiliation/40123/ ]

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:477647 (MONDO:equivalentTo)
  • MEDGEN:1842334 (MONDO:equivalentTo)
  • UMLS:C5681258 (MONDO:equivalentTo)
  • GARD:21957 (MONDO:GARD)
Subsets

gard_rare, rare, ordo_group_of_disorders

exactMatch

http://identifiers.org/medgen/1842334

http://linkedlifedata.com/resource/umls/id/C5681258

http://www.orpha.net/ORDO/Orphanet_477647

id

MONDO:0700264

term tracker item

https://github.com/monarch-initiative/mondo/issues/7365

Term relations