multicentric osteolysis-nodulosis-arthropathy spectrum
A rare genetic chronic skeletal disorder characterized by peripheral osteolysis (especially carpal and tarsal bones), interphalangeal joint erosions, subcutaneous fibrocollagenous nodules, facial dysmorphism, and a wide range of associated manifestations. [ Orphanet:371428 ]
Term info
- UMLS:CN227313 (MONDO:equivalentTo)
- SCTID:716868003 (MONDO:equivalentTo)
- Orphanet:371428 (MONDO:equivalentTo)
ordo_disease
A rare genetic chronic skeletal disorder characterized by peripheral osteolysis (especially carpal and tarsal bones), interphalangeal joint erosions, subcutaneous fibrocollagenous nodules, facial dysmorphism, and a wide range of associated manifestations.
http://identifiers.org/snomedct/716868003, http://purl.obolibrary.org/obo/Orphanet_371428, http://linkedlifedata.com/resource/umls/id/CN227313
mona spectrum
MONDO:0018298