716652006: Primary hepatic neuroendocrine carcinoma (disorder)

Descriptions:

Id Description Lang Type Status Case? Module

3307087011 Primary hepatic neuroendocrine carcinoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3307088018 Primary hepatic neuroendocrine carcinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3307089014 A rare hepatic tumor that may manifest with abdominal pain or fullness, as well as diarrhea or weight loss. More than 10% of cases are asymptomatic and in rare cases a carcinoid syndrome may be observed. The age of onset is variable. The etiology is still unknown but it is thought to arise from Kulchitsky cells originating in the neural crest. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

3307090017 A rare hepatic tumour that may manifest with abdominal pain or fullness, as well as diarrhoea or weight loss. More than 10% of cases are asymptomatic and in rare cases a carcinoid syndrome may be observed. The age of onset is variable. The aetiology is still unknown but it is thought to arise from Kulchitsky cells originating in the neural crest. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Primary hepatic neuroendocrine carcinoma (disorder)	Is a	Primary malignant neoplasm of liver	true	Inferred relationship	Some
Primary hepatic neuroendocrine carcinoma (disorder)	Is a	Neuroendocrine carcinoma	true	Inferred relationship	Some
Primary hepatic neuroendocrine carcinoma (disorder)	Associated morphology	Neuroendocrine tumor	false	Inferred relationship	Some	1
Primary hepatic neuroendocrine carcinoma (disorder)	Finding site	Liver structure	true	Inferred relationship	Some	1
Primary hepatic neuroendocrine carcinoma (disorder)	Associated morphology	Malignant neoplasm, primary	false	Inferred relationship	Some	2
Primary hepatic neuroendocrine carcinoma (disorder)	Finding site	Liver structure	false	Inferred relationship	Some	2
Primary hepatic neuroendocrine carcinoma (disorder)	Associated morphology	Neuroendocrine tumor	false	Inferred relationship	Some	2
Primary hepatic neuroendocrine carcinoma (disorder)	Pathological process (attribute)	Malignant proliferation of primary neoplasm (qualifier value)	false	Inferred relationship	Some	2
Primary hepatic neuroendocrine carcinoma (disorder)	Associated morphology	Neuroendocrine carcinoma	true	Inferred relationship	Some	1
Primary hepatic neuroendocrine carcinoma (disorder)	Pathological process (attribute)	Malignant proliferation of primary neoplasm (qualifier value)	true	Inferred relationship	Some	1
Primary hepatic neuroendocrine carcinoma (disorder)	Is a	Neuroendocrine neoplasm of liver (disorder)	true	Inferred relationship	Some
Primary hepatic neuroendocrine carcinoma (disorder)	Is a	Primary carcinoma liver and/or biliary system (disorder)	true	Inferred relationship	Some

Inbound Relationships

Characteristic

Refinability

Reference Sets

Id	Description	Lang	Type	Status	Case?	Module
3307087011	Primary hepatic neuroendocrine carcinoma (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3307088018	Primary hepatic neuroendocrine carcinoma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3307089014	A rare hepatic tumor that may manifest with abdominal pain or fullness, as well as diarrhea or weight loss. More than 10% of cases are asymptomatic and in rare cases a carcinoid syndrome may be observed. The age of onset is variable. The etiology is still unknown but it is thought to arise from Kulchitsky cells originating in the neural crest.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3307090017	A rare hepatic tumour that may manifest with abdominal pain or fullness, as well as diarrhoea or weight loss. More than 10% of cases are asymptomatic and in rare cases a carcinoid syndrome may be observed. The age of onset is variable. The aetiology is still unknown but it is thought to arise from Kulchitsky cells originating in the neural crest.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core