A congenital gingival tumor that occurs along the alveolar ridge of the maxilla. It usually affects female infants. The histogenesis is unknown. Morphologically, it is characterized by the presence of large cells with eosinophilic granular cytoplasm. Complete surgical resection is curative. [ NCIT:C4675 ]
Synonyms: congenital Epulides congenital gingival cell tumor congenital epulis congenital granular cell tumor congenital granular cell tumour congenital gingival cell tumour Neumann tumour Neumann tumor
Term information
- UMLS:C0376319 (MONDO:equivalentTo)
- GARD:20016 (MONDO:GARD)
- DOID:8303 (MONDO:equivalentTo)
- MESH:D005887 (MONDO:equivalentTo)
- NCIT:C4675 (MONDO:equivalentTo)
- SCTID:360525006 (MONDO:equivalentTo)
- MEDGEN:83962 (MONDO:equivalentTo)
- Orphanet:157826 (MONDO:equivalentTo)
- DOID:7280 (MONDO:equivalentTo)
ordo_disorder, gard_rare, rare, nord_rare, orphanet_rare
http://identifiers.org/mesh/D005887
http://purl.obolibrary.org/obo/DOID_7280
http://purl.obolibrary.org/obo/NCIT_C4675
http://identifiers.org/medgen/83962
http://www.orpha.net/ORDO/Orphanet_157826
http://purl.obolibrary.org/obo/DOID_8303
http://identifiers.org/snomedct/360525006
http://linkedlifedata.com/resource/umls/id/C0376319
https://github.com/monarch-initiative/mondo/issues/7284
https://github.com/monarch-initiative/mondo/issues/4069