Relapsing polychondritis (RP) is a rare, clinically heterogeneous, multisystemic inflammatory disease characterized by inflammation of the cartilage and proteoglycan rich structures leading to cartilage damage with joint, ocular and cardiovascular involvement. [ Orphanet:728 ]

This is just here as a test because I lose it

Term information

database cross reference
  • NCIT:C157268 (MONDO:equivalentTo)
  • MESH:D011081 (Orphanet:728)
  • MedDRA:10038304 (Orphanet:728)
  • UMLS:C0032453 (Orphanet:728)
  • ICD10:M94.1 (Orphanet:728)
  • SCTID:72275000 (MONDO:equivalentTo)
  • EFO:1001148 (MONDO:equivalentTo)
  • ICD9:733.99 (i2s)
  • DOID:2556 (MONDO:equivalentTo)
  • GARD:0007417 (MONDO:equivalentTo)
  • Orphanet:728 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease

closeMatch

http://identifiers.org/snomedct/111256009

http://identifiers.org/snomedct/85780006

definition

Relapsing polychondritis (RP) is a rare, clinically heterogeneous, multisystemic inflammatory disease characterized by inflammation of the cartilage and proteoglycan rich structures leading to cartilage damage with joint, ocular and cardiovascular involvement.

exactMatch

http://purl.obolibrary.org/obo/DOID_2556

http://identifiers.org/snomedct/72275000

http://purl.obolibrary.org/obo/NCIT_C157268

http://www.orpha.net/ORDO/Orphanet_728

http://identifiers.org/meddra/10038304

http://linkedlifedata.com/resource/umls/id/C0032453

http://identifiers.org/mesh/D011081

has exact synonym

chondromalacia, systemic

has related synonym

recurrent polychondritis

chronic atrophic polychondritis

id

MONDO:0019125

seeAlso

https://rarediseases.info.nih.gov/diseases/7417/relapsing-polychondritis