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764999002: Non-functioning paraganglioma (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3656012019 Non-functioning paraganglioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3656013012 Non-functioning paraganglioma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3656014018 Non-secreting paraganglioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5404454011 A rare neuroendocrine tumor arising from neural crest-derived paraganglion cells (most often in the para-aortic region at the level of renal hilum, organ of Zuckerkandl, thoracic paraspinal region, bladder, and carotid body) not associated with catecholamine secretion. These tumors are usually clinically silent and symptoms, if present, are nonspecific and depend on the location of the tumor. Association with certain hereditary cancer-predisposing syndromes, such as multiple endocrine neoplasia, neurofibromatosis type 1 or von Hippel Lindau syndrome, may be observed. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404455012 A rare neuroendocrine tumour arising from neural crest-derived paraganglion cells (most often in the para-aortic region at the level of renal hilum, organ of Zuckerkandl, thoracic paraspinal region, bladder, and carotid body) not associated with catecholamine secretion. These tumours are usually clinically silent and symptoms, if present, are nonspecific and depend on the location of the tumour. Association with certain hereditary cancer-predisposing syndromes, such as multiple endocrine neoplasia, neurofibromatosis type 1 or von Hippel Lindau syndrome, may be observed. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3656012019 Non-functioning paraganglioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3656013012 Non-functioning paraganglioma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3656014018 Non-secreting paraganglioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3655801014 A rare neuroendocrine neoplasm arising from neural crest-derived paraganglion cells (most often in the para-aortic region at the level of renal hilii, organ of Zuckerkandl, thoracic paraspinal region, bladder and carotid body) not associated with catecholamine secretion. These neoplasms are usually clinically silent and symptoms if present are nonspecific and depend on the location of the neoplasm. Association with certain hereditary cancer-predisposing syndromes, such as multiple endocrine neoplasia, neurofibromatosis type 1 or von Hippel lindau syndrome may be observed. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404454011 A rare neuroendocrine tumor arising from neural crest-derived paraganglion cells (most often in the para-aortic region at the level of renal hilum, organ of Zuckerkandl, thoracic paraspinal region, bladder, and carotid body) not associated with catecholamine secretion. These tumors are usually clinically silent and symptoms, if present, are nonspecific and depend on the location of the tumor. Association with certain hereditary cancer-predisposing syndromes, such as multiple endocrine neoplasia, neurofibromatosis type 1 or von Hippel Lindau syndrome, may be observed. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404455012 A rare neuroendocrine tumour arising from neural crest-derived paraganglion cells (most often in the para-aortic region at the level of renal hilum, organ of Zuckerkandl, thoracic paraspinal region, bladder, and carotid body) not associated with catecholamine secretion. These tumours are usually clinically silent and symptoms, if present, are nonspecific and depend on the location of the tumour. Association with certain hereditary cancer-predisposing syndromes, such as multiple endocrine neoplasia, neurofibromatosis type 1 or von Hippel Lindau syndrome, may be observed. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3412501001000115 Paragangliom, nicht-funktionelles de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
914281000172113 paragangliome non sécrétant fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
914281000172113 paragangliome non sécrétant fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3412501001000115 Paragangliom, nicht-funktionelles de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Non-functioning paraganglioma Associated morphology Paraganglioma true Inferred relationship Existential restriction modifier (core metadata concept) 1
Non-functioning paraganglioma Is a Paraganglioma (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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