Familial Mediterranean fever (FMF) is an autoinflammatory disorder characterized by recurrent short episodes of fever and serositis resulting in pain in the abdomen, chest, joints and muscles. [ Orphanet:342 ]

Synonyms: benign paroxysmal peritonitis benign recurrent polyserositis familial Mediterranean fever periodic disease FMF familial paroxysmal polyserositis

This is just here as a test because I lose it

Term information

database cross reference
  • NORD:1130 (MONDO:NORD)
  • ICD9:277.31 (MONDO:i2s)
  • UMLS:C0031069 (Orphanet:342/e)
  • MESH:D010505 (Orphanet:342/e)
  • DOID:2987 (MONDO:equivalentTo)
  • Orphanet:342 (MONDO:equivalentTo)
  • SCTID:12579009 (MONDO:equivalentTo)
  • NCIT:C84707 (MONDO:equivalentTo)
  • GARD:6421 (Orphanet:342)
  • MedDRA:10016207 (Orphanet:342/e)
Subsets

gard_rare, ordo_disease, rare, nord_rare, orphanet_rare, clingen

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/6747

closeMatch

http://identifiers.org/meddra/10016207

exactMatch

http://purl.obolibrary.org/obo/NCIT_C84707

http://purl.obolibrary.org/obo/DOID_2987

http://identifiers.org/snomedct/12579009

http://identifiers.org/mesh/D010505

http://www.orpha.net/ORDO/Orphanet_342

http://linkedlifedata.com/resource/umls/id/C0031069

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0019724

http://purl.obolibrary.org/obo/MONDO_0007179

id

MONDO:0018088

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0018088