FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

85583005: Pheochromocytoma (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
141864017 Pheochromocytoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
141866015 Chromaffin paraganglioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
141867012 Chromaffin tumor en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
141868019 Chromaffinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
141870011 Phaeochromocytoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
201225012 Adrenal medullary paraganglioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
506611012 Chromaffin tumour en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
827667018 Pheochromocytoma (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3782047015 Chromaffin cell neoplasm en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
141864017 Pheochromocytoma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
141864017 Pheochromocytoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
141866015 Chromaffin paraganglioma en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
141866015 Chromaffin paraganglioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
141867012 Chromaffin tumor en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
141867012 Chromaffin tumor en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
141868019 Chromaffinoma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
141868019 Chromaffinoma en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
141868019 Chromaffinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
141870011 Phaeochromocytoma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
141870011 Phaeochromocytoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
201225012 Adrenal medullary paraganglioma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
201225012 Adrenal medullary paraganglioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
506611012 Chromaffin tumour en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
506611012 Chromaffin tumour en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
827667018 Pheochromocytoma (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
827667018 Pheochromocytoma (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1235052014 [M]Phaeochromocytoma NOS en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3782047015 Chromaffin cell neoplasm en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pheochromocytoma Is a Neoplasm false Inferred relationship Existential restriction modifier (core metadata concept)
Pheochromocytoma Is a Chromaffin cell neoplasm false Inferred relationship Existential restriction modifier (core metadata concept)
Pheochromocytoma Is a Paraganglioma AND/OR glomus tumor (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Benign pheochromocytoma morphology Is a True Pheochromocytoma Inferred relationship Existential restriction modifier (core metadata concept)
Catecholamine secretion by pheochromocytoma Associated morphology False Pheochromocytoma Inferred relationship Existential restriction modifier (core metadata concept) 1
Pheochromocytoma (disorder) Associated morphology True Pheochromocytoma Inferred relationship Existential restriction modifier (core metadata concept) 1
Catecholamine secretion by pheochromocytoma Associated morphology True Pheochromocytoma Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare, hereditary, phaeochromocytoma/paraganglioma tumour arising from neuroendocrine chromaffin cells of the adrenal medulla (phaeochromocytoma) or from any paraganglia from the skull base to the pelvic floor (paraganglioma). Clinical manifestations are often linked to excess catecholamines production causing sustained or paroxysmal elevations in blood pressure, headache, episodic profuse sweating, palpitations, pallor and apprehension or anxiety. Hereditary phaeochromocytoma/paraganglioma tumours tend to present at younger ages, to be multi-focal, bilateral, and recurrent, or to have multiple synchronous neoplasms. Associated morphology True Pheochromocytoma Inferred relationship Existential restriction modifier (core metadata concept) 2
Phaeochromocytoma crisis Associated morphology True Pheochromocytoma Inferred relationship Existential restriction modifier (core metadata concept) 1
Sporadic pheochromocytoma and secreting paraganglioma Associated morphology True Pheochromocytoma Inferred relationship Existential restriction modifier (core metadata concept) 2
Malignant pheochromocytoma Is a True Pheochromocytoma Inferred relationship Existential restriction modifier (core metadata concept)
Composite pheochromocytoma (morphologic abnormality) Is a True Pheochromocytoma Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start