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764999002: Non-functioning paraganglioma (disorder)


Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3656012019 Non-functioning paraganglioma en Synonym Active Case insensitive SNOMED CT core
3656013012 Non-functioning paraganglioma (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3656014018 Non-secreting paraganglioma en Synonym Active Case insensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Non-functioning paraganglioma Associated morphology Paraganglioma true Inferred relationship Some 1
Non-functioning paraganglioma Is a Paraganglioma true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Neoplasm and/or hamartoma reference set

Problem/Diagnosis reference set

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