Term info
- ICD10CM:D44.8 (Orphanet:1359/ntbt)
- NCIT:C4705 (MONDO:equivalentTo)
- SCTID:733491005 (MONDO:equivalentTo)
- DOID:0050471 (MONDO:equivalentTo)
- GARD:0001119 (MONDO:equivalentTo)
- MESH:D056733 (Orphanet:1359/e)
- UMLS:C0406810 (Orphanet:1359/e)
- Orphanet:1359 (MONDO:equivalentTo)
ordo_disease
Carney complex (CNC) is characterized by spotty skin pigmentation, endocrine overactivity and myxomas.
http://identifiers.org/snomedct/733491005, http://purl.obolibrary.org/obo/Orphanet_1359, http://identifiers.org/mesh/D056733, http://linkedlifedata.com/resource/umls/id/C0406810, http://purl.obolibrary.org/obo/NCIT_C4705, http://purl.obolibrary.org/obo/DOID_0050471
lamb syndrome, Carney syndrome, Myxoma-spotty pigmentation-endocrine overactivity syndrome, lamb, NAME syndrome, CNC, Carney's syndrome, atrial myxoma with lentigines, nevi, atrial myxoma, skin myxoma, ephelides syndrome, lentigines, atrial myxoma, mucocutaneous myoma, blue Nevus syndrome, Carney complex
Carney Complex, type 1, Carney Complex, type 2
Myxoma - spotty pigmentation - endocrine overactivity
MONDO:0015285
http://purl.bioontology.org/ontology/ICD10CM/D44.8
Term relations
- autosomal dominant disease
- disease has feature some hyperpigmentation of the skin
- disease has feature some inherited cardiac tumor
- disease has feature some palpebral lentiginosis
- disease has feature some adrenal gland neoplasm
- disease has feature some multiple polyglandular tumor
- disease has feature some mesenchymatous palpebral tumor