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1222643003: Hereditary malignant neuroendocrine neoplasm of small intestine (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5048267015 Hereditary malignant neuroendocrine tumor of small intestine en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5048268013 Hereditary malignant neuroendocrine neoplasm of small intestine (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5048269017 Hereditary malignant neuroendocrine tumour of small intestine en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5048270016 Hereditary malignant neuroendocrine tumour of small bowel en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5048271017 Hereditary malignant neuroendocrine tumor of small bowel en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5048274013 Hereditary malignant neuroendocrine neoplasm of small intestine en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5048272012 A rare inherited cancer-predisposing syndrome characterized by occurrence of multiple synchronous primary carcinoids of the small intestine. Clinical presentation is otherwise indistinguishable from sporadic carcinoids and includes abdominal pain, flushing, and diarrhea, often becoming manifest only after a long asymptomatic period. Most patients present with low grade tumors. Occurrence of pulmonary carcinoids has also been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5048273019 A rare inherited cancer-predisposing syndrome characterised by occurrence of multiple synchronous primary carcinoids of the small intestine. Clinical presentation is otherwise indistinguishable from sporadic carcinoids and includes abdominal pain, flushing, and diarrhoea, often becoming manifest only after a long asymptomatic period. Most patients present with low grade tumours. Occurrence of pulmonary carcinoids has also been reported. 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
Hereditary malignant neuroendocrine neoplasm of small intestine (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Hereditary malignant neuroendocrine neoplasm of small intestine (disorder) Is a Gastrointestinal hormone-secreting endocrine tumor true Inferred relationship Some
Hereditary malignant neuroendocrine neoplasm of small intestine (disorder) Is a Carcinoid tumor of small intestine true Inferred relationship Some
Hereditary malignant neuroendocrine neoplasm of small intestine (disorder) Is a Digestive system hereditary disorder (disorder) true Inferred relationship Some
Hereditary malignant neuroendocrine neoplasm of small intestine (disorder) Is a Malignant tumor of small intestine true Inferred relationship Some
Hereditary malignant neuroendocrine neoplasm of small intestine (disorder) Is a Hereditary cancer-predisposing syndrome true Inferred relationship Some
Hereditary malignant neuroendocrine neoplasm of small intestine (disorder) Finding site Structure of small intestine (body structure) true Inferred relationship Some 1
Hereditary malignant neuroendocrine neoplasm of small intestine (disorder) Associated morphology Malignant carcinoid tumor true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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