Term info
- UMLS:C0524988 (Orphanet:37748/e)
- SCTID:402415001 (MONDO:equivalentTo)
- EFO:1001165 (MONDO:equivalentTo)
- DOID:4371 (MONDO:equivalentTo)
- MedDRA:10062908 (Orphanet:37748/e)
- GARD:0012390 (MONDO:equivalentTo)
- ICD9:708.8 (MONDO:relatedTo)
- Orphanet:37748 (MONDO:equivalentTo)
- MESH:D019873 (Orphanet:37748/e)
gard_rare, ordo_malformation_syndrome
http://identifiers.org/meddra/10062908
A rare, underdiagnosed disorder in adults characterized by recurrent febrile rash, bone and/or joint pain, enlarged lymph nodes, fatigue, a monoclonal IgM component, leukocytosis and systemic inflammatory response.
http://purl.obolibrary.org/obo/Orphanet_37748, http://linkedlifedata.com/resource/umls/id/C0524988, http://identifiers.org/mesh/D019873, http://identifiers.org/snomedct/402415001, http://purl.obolibrary.org/obo/DOID_4371
http://purl.obolibrary.org/obo/MONDO_0002459, http://purl.obolibrary.org/obo/MONDO_0015158, http://purl.obolibrary.org/obo/MONDO_0005492
chronic urticaria with gammopathy, chronic urticaria with macroglobulinemia
chronic urticaria with gammapathy
MONDO:0018304
https://rarediseases.info.nih.gov/diseases/12390/schnitzler-syndrome