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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
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
5172249014 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
5172250014 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
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
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). Is a Gastrointestinal hormone-secreting endocrine tumor false Inferred relationship Existential restriction modifier (core metadata concept)
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). Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
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). Is a Malignant neoplasm of stomach (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
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). Is a Familial neoplastic disease true Inferred relationship Existential restriction modifier (core metadata concept)
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). Is a Neuroendocrine neoplasm of stomach (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
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). Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
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). Finding site Stomach structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
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). Associated morphology Neuroendocrine tumor false Inferred relationship Existential restriction modifier (core metadata concept) 1
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). Associated morphology Well-differentiated neuroendocrine tumor (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
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). Is a Well-differentiated neuroendocrine tumor of stomach (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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