SNOMED CT

Last uploaded: January 31, 2024
Preferred Name

Pheochromocytoma

Synonyms

Pheochromocytoma (disorder)

Chromaffin tumor

ID

http://purl.bioontology.org/ontology/SNOMEDCT/302835009

Active

1

altLabel

Pheochromocytoma (disorder)

Chromaffin paraganglioma

Adrenal medullary paraganglioma

Chromaffin tumour

Phaeochromocytoma

Chromaffinoma

Chromaffin tumor

Associated finding of

http://purl.bioontology.org/ontology/SNOMEDCT/3640001000004101

http://purl.bioontology.org/ontology/SNOMEDCT/49221000119108

CASE SIGNIFICANCE ID

900000000000020002

900000000000448009

Cause of

http://purl.bioontology.org/ontology/SNOMEDCT/1156847004

http://purl.bioontology.org/ontology/SNOMEDCT/403259002

CTV3ID

Xa99P

cui

C4551683

DEFINITION STATUS ID

900000000000073002

Effective time

20030731

Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/85583005

INACTIVATION INDICATOR

900000000000495008

900000000000484002

notation

302835009

prefLabel

Pheochromocytoma

Subset member

6011000124106~MAPRULE~IFA 716857003 | Hereditary pheochromocytoma and paraganglioma |

900000000000497000~MAPTARGET~Xa99P

447562003~MAPRULE~TRUE

6011000124106~MAPRULE~IFA 1079411000119102 | Benign pheochromocytoma of left adrenal gland |

6011000124106~MAPTARGET~D35.02

6011000124106~MAPPRIORITY~4

6011000124106~MAPTARGET~D44.7

900000000000489007~VALUEID~900000000000484002

6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA

900000000000523009~TARGETCOMPONENT~360332001

6011000124106~MAPTARGET~

6011000124106~MAPCATEGORYID~447638001

6011000124106~MAPADVICE~IF HEREDITARY PHEOCHROMOCYTOMA AND PARAGANGLIOMA CHOOSE D44.7 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPTARGET~D35.0

6011000124106~MAPRULE~IFA 76564002 | Catecholamine secretion by pheochromocytoma (disorder) |

6011000124106~MAPGROUP~1

6011000124106~MAPGROUP~2

6011000124106~MAPADVICE~IF SPORADIC PHEOCHROMOCYTOMA AND SECRETING PARAGANGLIOMA CHOOSE D44.7 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF BENIGN PHEOCHROMOCYTOMA OF LEFT ADRENAL GLAND CHOOSE D35.02 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000490003~VALUEID~900000000000495008

900000000000508004~ACCEPTABILITYID~900000000000549004

447562003~MAPGROUP~1

6011000124106~MAPTARGET~D35.00

6011000124106~MAPTARGET~D35.01

447562003~CORRELATIONID~447561005

6011000124106~MAPADVICE~ALWAYS D35.00 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | CONSIDER LATERALITY SPECIFICATION | DESCENDANTS NOT EXHAUSTIVELY MAPPED

6011000124106~MAPRULE~IFA 716857003 | Hereditary pheochromocytoma and paraganglioma (disorder) |

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPTARGET~C7A.8

6011000124106~MAPRULE~IFA 765143008 | Sporadic pheochromocytoma and secreting paraganglioma |

900000000000508004~ACCEPTABILITYID~900000000000548007

6011000124106~MAPADVICE~IF CATECHOLAMINE SECRETION BY PHEOCHROMOCYTOMA CHOOSE E27.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPPRIORITY~5

6011000124106~MAPADVICE~IF BENIGN PHEOCHROMOCYTOMA OF RIGHT ADRENAL GLAND CHOOSE D35.01 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~E27.5

6011000124106~MAPCATEGORYID~447639009

6011000124106~MAPADVICE~ALWAYS D35.00 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | CONSIDER LATERALITY SPECIFICATION

6011000124106~MAPADVICE~IF MALIGNANT PHEOCHROMOCYTOMA CHOOSE C7A.8 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~1

6011000124106~CORRELATIONID~447561005

6011000124106~MAPRULE~IFA 1079421000119109 | Benign pheochromocytoma of right adrenal gland |

6011000124106~MAPRULE~IFA 76564002 | Catecholamine secretion by pheochromocytoma |

6011000124106~MAPRULE~TRUE

6011000124106~MAPRULE~IFA 21851000119103 | Malignant pheochromocytoma |

6011000124106~MAPPRIORITY~3

447562003~MAPADVICE~ALWAYS D35.0 | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPPRIORITY~2

900000000000523009~TARGETCOMPONENT~360335004

tui

T191

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/255046005

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MDRGER/10034876 MDRGER CUI
http://purl.bioontology.org/ontology/RCD/Xa99P RCD CUI
http://purl.bioontology.org/ontology/RCD/BBD9. RCD CUI
http://purl.bioontology.org/ontology/SCTSPA/85583005 SCTSPA CUI
http://purl.bioontology.org/ontology/MEDDRA/10034876 MEDDRA CUI
http://purl.bioontology.org/ontology/MDRFRE/10034800 MDRFRE CUI
http://purl.bioontology.org/ontology/MEDDRA/10034800 MEDDRA CUI
http://purl.bioontology.org/ontology/OMIM/MTHU004454 OMIM CUI
http://purl.bioontology.org/ontology/OMIM/MTHU067042 OMIM CUI
http://purl.bioontology.org/ontology/CSP/2012-7663 CRISP CUI
http://purl.bioontology.org/ontology/MDRGER/10034800 MDRGER CUI
http://purl.bioontology.org/ontology/MDRFRE/10034876 MDRFRE CUI
http://purl.bioontology.org/ontology/SCTSPA/302835009 SCTSPA CUI
http://purl.obolibrary.org/obo/HP_0002666 HP LOOM
http://purl.obolibrary.org/obo/HP_0002666 HP LOOM
http://purl.obolibrary.org/obo/DOID_0050771 DOID LOOM
http://purl.obolibrary.org/obo/MONDO_0008233 MONDO LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0031511 OCHV LOOM
http://purl.bioontology.org/ontology/MEDDRA/10034876 MEDDRA LOOM
http://purl.jp/bio/4/id/200906031583220746 IOBC LOOM
http://purl.obolibrary.org/obo/DERMO_0002049 DERMO LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#9623 OCHV LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C04.557.465.625.650.700.725 RH-MESH LOOM
http://bmi.utah.edu/ontologies/hfontology/C0031511 HFO LOOM
http://radlex.org/RID/RID4516 RADLEX LOOM
http://purl.bioontology.org/ontology/PDQ/CDR0000039816 PDQ LOOM
http://purl.obolibrary.org/obo/DOID_0050771 BAO LOOM
http://purl.obolibrary.org/obo/DOID_0050771 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_0050771 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_0050771 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_0050771 FNS-H LOOM
http://purl.org/obo/owl/HP#HP_0002666 BDO LOOM
http://purl.obolibrary.org/obo/OMIM_171300 CCO LOOM
http://purl.obolibrary.org/obo/OGMD_0000048 OGMD LOOM
http://purl.bioontology.org/ontology/MESH/D010673 MESH LOOM
http://www.phoc.org.cn/pmo/class/PMO_00085364 PMAPP-PMO LOOM
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:2458 IFAR LOOM
http://purl.obolibrary.org/obo/MONDO_0008233 DOVES LOOM
http://purl.obolibrary.org/obo/MPATH_377 MPATH LOOM
http://purl.obolibrary.org/obo/MPATH_377 UPHENO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D010673 RH-MESH LOOM
http://purl.obolibrary.org/obo/OMIT_0011661 OMIT LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0031511 MEDLINEPLUS LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU015027 OMIM LOOM
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:2311 IFAR LOOM
http://purl.bioontology.org/ontology/OMIM/171300 OMIM LOOM
http://doe-generated-ontology.com/OntoAD#C0031511 ONTOAD LOOM
http://purl.bioontology.org/ontology/CSP/2012-7663 CRISP LOOM
http://purl.bioontology.org/ontology/ICPC2P/T73008 ICPC2P LOOM
http://www.gamuts.net/entity#pheochromocytoma GAMUTS LOOM
http://identifiers.org/omim/171300 REXO LOOM
http://identifiers.org/omim/171300 GEXO LOOM
http://identifiers.org/omim/171300 RETO LOOM
http://purl.obolibrary.org/obo/HP_0002666 UPHENO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C04.557.580.625.650.700.725 RH-MESH LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Pheochromocytoma CSEO LOOM
http://www.gamuts.net/entity#pheochromocytoma GAMUTS REST