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1264340007: Familial gastric type 1 neuroendocrine neoplasm (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5172244016 Familial gastric type 1 neuroendocrine tumor en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5172245015 Familial gastric type 1 neuroendocrine neoplasm en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5172246019 Familial gastric type 1 neuroendocrine neoplasm (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5172247011 Familial gastric type 1 neuroendocrine tumour en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5400473016 A rare neoplastic disease characterized by occurrence of atypical and aggressive gastric type 1 neuroendocrine tumors (NET) in early adulthood. The tumors often show nodal infiltration requiring total gastrectomy. Synchronous gastric adenocarcinoma has also been reported. Patients present high serum gastrin concentrations and iron-deficiency anemia (rather than megaloblastic anemia, which is a typical feature in patients with sporadic gastric type 1 NET, where the tumor usually arises on the background of autoimmune atrophic gastritis). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400474010 A rare neoplastic disease characterised by occurrence of atypical and aggressive gastric type 1 neuroendocrine tumours (NET) in early adulthood. The tumours often show nodal infiltration requiring total gastrectomy. Synchronous gastric adenocarcinoma has also been reported. Patients present high serum gastrin concentrations and iron-deficiency anaemia (rather than megaloblastic anaemia, which is a typical feature in patients with sporadic gastric type 1 NET, where the tumour usually arises on the background of autoimmune atrophic gastritis). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial gastric type 1 neuroendocrine neoplasm Is a Gastrointestinal hormone-secreting endocrine tumor false Inferred relationship Some
Familial gastric type 1 neuroendocrine neoplasm Is a Digestive system hereditary disorder (disorder) true Inferred relationship Some
Familial gastric type 1 neuroendocrine neoplasm Is a Malignant neoplasm of stomach (disorder) false Inferred relationship Some
Familial gastric type 1 neuroendocrine neoplasm Is a Familial neoplastic disease true Inferred relationship Some
Familial gastric type 1 neuroendocrine neoplasm Is a Neuroendocrine neoplasm of stomach (disorder) false Inferred relationship Some
Familial gastric type 1 neuroendocrine neoplasm Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Familial gastric type 1 neuroendocrine neoplasm Finding site Stomach structure true Inferred relationship Some 1
Familial gastric type 1 neuroendocrine neoplasm Associated morphology Neuroendocrine tumor false Inferred relationship Some 1
Familial gastric type 1 neuroendocrine neoplasm Associated morphology Well-differentiated neuroendocrine tumor (morphologic abnormality) true Inferred relationship Some 1
Familial gastric type 1 neuroendocrine neoplasm Is a Well-differentiated neuroendocrine tumour of stomach true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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