embryonal carcinoma
A non-seminomatous malignant germ cell tumor characterized by the presence of large germ cells with abundant cytoplasm resembling epithelial cells, geographic necrosis, high mitotic activity, and pseudoglandular and pseudopapillary structures formation. It can arise from the testis, ovary, and extragonadal sites (central nervous system and mediastinum). [ NCIT:C3752 ]
Term info
- ICDO:9070/3 (NCIT:C3752)
- DOID:3308 (MONDO:equivalentTo)
- GARD:0005140 (MONDO:equivalentTo)
- MESH:D018236 (Orphanet:180226/e)
- EFO:0004986 (MONDO:equivalentTo)
- UMLS:C0206659 (Orphanet:180226/e)
- ONCOTREE:EMBCA (MONDO:equivalentTo)
- NCIT:C3752 (MONDO:equivalentTo)
- Orphanet:180226 (MONDO:equivalentTo)
gard_rare, ordo_disease
Editor note: TODO check classification w.r.t carcinoma
A non-seminomatous malignant germ cell tumor characterized by the presence of large germ cells with abundant cytoplasm resembling epithelial cells, geographic necrosis, high mitotic activity, and pseudoglandular and pseudopapillary structures formation. It can arise from the testis, ovary, and extragonadal sites (central nervous system and mediastinum).
http://purl.obolibrary.org/obo/Orphanet_180226, http://purl.obolibrary.org/obo/NCIT_C3752, http://identifiers.org/mesh/D018236, http://linkedlifedata.com/resource/umls/id/C0206659, http://purl.obolibrary.org/obo/DOID_3308
http://purl.obolibrary.org/obo/MONDO_0004993
carcinoma, embryonal, malignant, embryonal carcinoma
primary extragonadal embryonal carcinoma
MONDO:0005440
https://rarediseases.info.nih.gov/diseases/5140/embryonal-carcinoma