Carney triad
Carney's triad is a rare non-hereditary condition characterized by gastrointestinal stromal tumors (GIST, intramural mesenchymal tumors of the gastrointestinal tract with neuronal or neural crest cell origin), pulmonary chondromas and extraadrenal paragangliomas. [ Orphanet:139411 ]
Term info
- NCIT:C94833 (MONDO:equivalentTo)
- SCTID:733492003 (MONDO:equivalentTo)
- Orphanet:139411 (OMIM:604287)
- UMLS:C1858592 (Orphanet:139411)
- OMIM:604287 (Orphanet:139411/e)
- GARD:0010924 (MONDO:equivalentTo)
- MESH:C565803 (MONDO:equivalentTo)
gard_rare, ordo_disease
Carney's triad is a rare non-hereditary condition characterized by gastrointestinal stromal tumors (GIST, intramural mesenchymal tumors of the gastrointestinal tract with neuronal or neural crest cell origin), pulmonary chondromas and extraadrenal paragangliomas.
http://identifiers.org/snomedct/733492003, http://purl.obolibrary.org/obo/NCIT_C94833, http://identifiers.org/mesh/C565803, http://purl.obolibrary.org/obo/Orphanet_139411, http://linkedlifedata.com/resource/umls/id/C1858592, https://omim.org/entry/604287
Carney triad
gastric leiomyosarcoma, pulmonary chondroma, and extraadrenal paraganglioma
MONDO:0011424
https://rarediseases.info.nih.gov/diseases/10924/carney-triad