SNOMED CT

Last uploaded: January 31, 2024
Preferred Name

Insulinoma

Synonyms

Insulinoma (disorder)

Beta cell adenoma

Definitions

A form of functioning pancreatic neuroendocrine tumour characterised most commonly by a solitary, small pancreatic lesion that causes hyperinsulinaemic hypoglycaemia. Insulinoma can present at any age but the median age of diagnosis is in the fifth decade of life. Insulinoma is malignant in only 7-10% of cases and the most common sites of metastasis are the liver and lymph nodes. The aetiology is unknown in most sporadic cases but somatic YY1 (14q32.2) variants are associated with insulinoma in some cases. Insulinoma originates in the islet beta cells that are equally distributed throughout the pancreas. When functioning, the tumour manifests with hypersecretion of insulin and consequently causes hypoglycaemia. With the exception of insulinoma in MEN1, insulinoma is not hereditary.

ID

http://purl.bioontology.org/ontology/SNOMEDCT/302822000

Active

1

altLabel

Insulinoma (disorder)

Beta cell adenoma

CASE SIGNIFICANCE ID

900000000000448009

CTV3ID

Xa98M

cui

C0021670

definition

A form of functioning pancreatic neuroendocrine tumour characterised most commonly by a solitary, small pancreatic lesion that causes hyperinsulinaemic hypoglycaemia. Insulinoma can present at any age but the median age of diagnosis is in the fifth decade of life. Insulinoma is malignant in only 7-10% of cases and the most common sites of metastasis are the liver and lymph nodes. The aetiology is unknown in most sporadic cases but somatic YY1 (14q32.2) variants are associated with insulinoma in some cases. Insulinoma originates in the islet beta cells that are equally distributed throughout the pancreas. When functioning, the tumour manifests with hypersecretion of insulin and consequently causes hypoglycaemia. With the exception of insulinoma in MEN1, insulinoma is not hereditary.

A form of functioning pancreatic neuroendocrine tumor characterized most commonly by a solitary, small pancreatic lesion that causes hyperinsulinemic hypoglycemia. Insulinoma can present at any age but the median age of diagnosis is in the fifth decade of life. Insulinoma is malignant in only 7-10% of cases and the most common sites of metastasis are the liver and lymph nodes. The etiology is unknown in most sporadic cases but somatic YY1 (14q32.2) variants are associated with insulinoma in some cases. Insulinoma originates in the islet beta cells that are equally distributed throughout the pancreas. When functioning, the tumor manifests with hypersecretion of insulin and consequently causes hypoglycemia. With the exception of insulinoma in MEN1, insulinoma is not hereditary.

DEFINITION STATUS ID

900000000000074008

Effective time

20230228

Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/128928004

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/15776009

INACTIVATION INDICATOR

900000000000495008

900000000000484002

notation

302822000

prefLabel

Insulinoma

Subset member

447562003~MAPRULE~TRUE

6011000124106~MAPTARGET~D37.8

900000000000523009~TARGETCOMPONENT~713189001

900000000000489007~VALUEID~900000000000484002

6011000124106~MAPGROUP~1

6011000124106~MAPADVICE~IF MALIGNANT INSULINOMA CHOOSE C25.4 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA

447562003~MAPTARGET~D13.7

6011000124106~MAPTARGET~C25.4

900000000000490003~VALUEID~900000000000495008

900000000000508004~ACCEPTABILITYID~900000000000549004

447562003~MAPGROUP~1

447562003~CORRELATIONID~447561005

6011000124106~MAPCATEGORYID~447637006

447562003~MAPADVICE~ALWAYS D37.7 | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPADVICE~ALWAYS D37.8

900000000000508004~ACCEPTABILITYID~900000000000548007

447562003~MAPTARGET~

6011000124106~MAPRULE~IFA 713189001 | Malignant insulinoma (disorder) |

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

6011000124106~MAPRULE~OTHERWISE TRUE

447562003~MAPTARGET~D37.7

6011000124106~MAPCATEGORYID~447639009

900000000000497000~MAPTARGET~Xa98M

447562003~MAPADVICE~ALWAYS D13.7 | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE

900000000000523009~TARGETCOMPONENT~788390005

6011000124106~MAPPRIORITY~1

6011000124106~CORRELATIONID~447561005

6011000124106~MAPRULE~TRUE

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPPRIORITY~2

447562003~MAPCATEGORYID~447638001

tui

T191

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/717919005

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/NDFRT/N0000001693 NDFRT CUI
http://purl.bioontology.org/ontology/PDQ/CDR0000038792 PDQ CUI
http://purl.bioontology.org/ontology/MESH/D007340 MESH CUI
http://purl.bioontology.org/ontology/SNMI/M-81510 SNMI CUI
http://purl.bioontology.org/ontology/OMIM/MTHU018340 OMIM CUI
http://purl.bioontology.org/ontology/CSP/2014-4965 CRISP CUI
http://purl.bioontology.org/ontology/RCD/BB5B2 RCD CUI
http://purl.bioontology.org/ontology/MDRFRE/10022498 MDRFRE CUI
http://purl.bioontology.org/ontology/RCD/Xa98M RCD CUI
http://purl.bioontology.org/ontology/SCTSPA/302822000 SCTSPA CUI
http://purl.bioontology.org/ontology/MDRGER/10022498 MDRGER CUI
http://purl.bioontology.org/ontology/MEDDRA/10022498 MEDDRA CUI
http://purl.bioontology.org/ontology/MSHFRE/D007340 MSHFRE CUI
http://purl.bioontology.org/ontology/PDQ/CDR0000040018 PDQ CUI
http://purl.bioontology.org/ontology/ICPC2P/T73009 ICPC2P CUI
http://purl.obolibrary.org/obo/HP_0012197 HP LOOM
http://purl.obolibrary.org/obo/HP_0012197 HP LOOM
http://www.ebi.ac.uk/efo/EFO_0000549 EFO LOOM
http://purl.obolibrary.org/obo/DOID_3892 DOID LOOM
http://purl.jp/bio/4/id/200906007024595650 IOBC LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C04.588.322.475.249.500 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C19.344.421.249.500 RH-MESH LOOM
http://www.phoc.org.cn/pmo/class/PMO_00085660 PMAPP-PMO LOOM
http://purl.bioontology.org/ontology/PDQ/CDR0000038792 PDQ LOOM
http://purl.bioontology.org/ontology/MESH/D007340 MESH LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_3903 NATPRO LOOM
http://radlex.org/RID/RID4486 RADLEX LOOM
http://localhost/plosthes.2017-1#7560 PLOSTHES LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D007340 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C04.557.470.035.100.852 RH-MESH LOOM
http://purl.obolibrary.org/obo/HP_0012197 UPHENO LOOM
http://purl.obolibrary.org/obo/DERMO_0002668 DERMO LOOM
http://www.orpha.net/ORDO/Orphanet_97279 ORDO LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#6789 OCHV LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C06.689.667.249.500 RH-MESH LOOM
http://www.gamuts.net/entity#insulinoma GAMUTS LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU018340 OMIM LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C04.588.274.761.249.500 RH-MESH LOOM
http://purl.bioontology.org/ontology/RCD/Xa98M RCD LOOM
http://www.ebi.ac.uk/efo/EFO_0000549 OBI_BCGO LOOM
http://purl.obolibrary.org/obo/DOID_3892 DTO LOOM
http://purl.obolibrary.org/obo/DOID_3892 BAO LOOM
http://purl.obolibrary.org/obo/DOID_3892 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_3892 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_3892 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_3892 FNS-H LOOM
http://www.limics.org/hrdo/rdfns#pat_id_12875 HRDO LOOM
http://purl.bioontology.org/ontology/MEDDRA/10022498 MEDDRA LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0021670 OCHV LOOM
http://purl.obolibrary.org/obo/OMIT_0008458 OMIT LOOM
http://id.nlm.nih.gov/mesh/D007340 MDM LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C06.301.761.249.500 RH-MESH LOOM
http://purl.bioontology.org/ontology/ICPC2P/T73009 ICPC2P LOOM
http://www.gamuts.net/entity#insulinoma GAMUTS REST