pancreatic neuroendocrine tumor glucagonoma https://www.malacards.org/card/glucagonoma SCTID:16424000 NANDO:2100142 Glucagonoma is a rare, functioning type of pancreatic neuroendocrine tumor (PNET) that hypersecretes glucagon, leading to a syndrome comprised of necrolytic migratory erythema, diabetes mellitus, anemia, weight loss, mucosal abnormalities, thromboembolism, gastrointestinal and neuropsychiatric symptoms. icd11.foundation:1918063179 UMLS:C0017689 NCIT:C95597 pancreatic glucagonoma MEDGEN:4908 glucagonoma syndrome Orphanet:97280 MedDRA:10018404 icd11.foundation:2121897507 MONDO:0019959 NANDO:2200397 GARD:0002496 glucagonoma MESH:D005935