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716859000: Hereditary diffuse carcinoma of stomach (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3307807012 Hereditary diffuse carcinoma of stomach (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307808019 Hereditary diffuse carcinoma of stomach en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307809010 Hereditary diffuse gastric cancer en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3529910014 Familial diffuse gastric cancer en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3529911013 E-cadherin-associated hereditary gastric cancer en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401418011 Hereditary diffuse gastric cancer is a rare epithelial tumor of the stomach, characterized by the development of diffuse (signet ring cell) gastric cancer at a young age, associated with germline heterozygous mutations of CDH1, MAP3K6 and CTNNA1 genes. In early stages it presents with non-specific and vague symptoms, in advanced stages it may cause nausea and vomiting, dysphagia, loss of appetite, abdominal mass or weight loss. Women have an increased risk of lobular breast cancer as well. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401419015 Hereditary diffuse gastric cancer is a rare epithelial tumour of the stomach, characterised by the development of diffuse (signet ring cell) gastric cancer at a young age, associated with germline heterozygous mutations of CDH1, MAP3K6 and CTNNA1 genes. In early stages it presents with non-specific and vague symptoms, in advanced stages it may cause nausea and vomiting, dysphagia, loss of appetite, abdominal mass or weight loss. Women have an increased risk of lobular breast cancer as well. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3307807012 Hereditary diffuse carcinoma of stomach (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307807012 Hereditary diffuse carcinoma of stomach (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307808019 Hereditary diffuse carcinoma of stomach en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307808019 Hereditary diffuse carcinoma of stomach en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307809010 Hereditary diffuse gastric cancer en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307809010 Hereditary diffuse gastric cancer en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3529910014 Familial diffuse gastric cancer en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3529911013 E-cadherin-associated hereditary gastric cancer en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3307810017 Familial gastric cancer refers to the occurrence of gastric cancer in a familial context and is described as two or more cases of gastric cancer in first or second degree relatives with at least one case diagnosed before the age of 50. Familial clustering is observed in 10% of all cases of gastric cancer. Familial gastric cancer can also occur in other hereditary cancer syndromes such as Lynch syndrome and Li-Fraumeni syndrome. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401418011 Hereditary diffuse gastric cancer is a rare epithelial tumor of the stomach, characterized by the development of diffuse (signet ring cell) gastric cancer at a young age, associated with germline heterozygous mutations of CDH1, MAP3K6 and CTNNA1 genes. In early stages it presents with non-specific and vague symptoms, in advanced stages it may cause nausea and vomiting, dysphagia, loss of appetite, abdominal mass or weight loss. Women have an increased risk of lobular breast cancer as well. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401419015 Hereditary diffuse gastric cancer is a rare epithelial tumour of the stomach, characterised by the development of diffuse (signet ring cell) gastric cancer at a young age, associated with germline heterozygous mutations of CDH1, MAP3K6 and CTNNA1 genes. In early stages it presents with non-specific and vague symptoms, in advanced stages it may cause nausea and vomiting, dysphagia, loss of appetite, abdominal mass or weight loss. Women have an increased risk of lobular breast cancer as well. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3411501001000113 Magenkarzinom, diffuses hereditäres de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6285651000241111 carcinome héréditaire diffus de l'estomac fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6285661000241114 carcinome gastrique héréditaire diffus fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6285651000241111 carcinome héréditaire diffus de l'estomac fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6285661000241114 carcinome gastrique héréditaire diffus fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3411501001000113 Magenkarzinom, diffuses hereditäres de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary diffuse gastric cancer is a rare epithelial tumor of the stomach, characterized by the development of diffuse (signet ring cell) gastric cancer at a young age, associated with germline heterozygous mutations of CDH1, MAP3K6 and CTNNA1 genes. In early stages it presents with non-specific and vague symptoms, in advanced stages it may cause nausea and vomiting, dysphagia, loss of appetite, abdominal mass or weight loss. Women have an increased risk of lobular breast cancer as well. Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary diffuse gastric cancer is a rare epithelial tumor of the stomach, characterized by the development of diffuse (signet ring cell) gastric cancer at a young age, associated with germline heterozygous mutations of CDH1, MAP3K6 and CTNNA1 genes. In early stages it presents with non-specific and vague symptoms, in advanced stages it may cause nausea and vomiting, dysphagia, loss of appetite, abdominal mass or weight loss. Women have an increased risk of lobular breast cancer as well. Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary diffuse gastric cancer is a rare epithelial tumor of the stomach, characterized by the development of diffuse (signet ring cell) gastric cancer at a young age, associated with germline heterozygous mutations of CDH1, MAP3K6 and CTNNA1 genes. In early stages it presents with non-specific and vague symptoms, in advanced stages it may cause nausea and vomiting, dysphagia, loss of appetite, abdominal mass or weight loss. Women have an increased risk of lobular breast cancer as well. Is a Primary malignant neoplasm of stomach (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary diffuse gastric cancer is a rare epithelial tumor of the stomach, characterized by the development of diffuse (signet ring cell) gastric cancer at a young age, associated with germline heterozygous mutations of CDH1, MAP3K6 and CTNNA1 genes. In early stages it presents with non-specific and vague symptoms, in advanced stages it may cause nausea and vomiting, dysphagia, loss of appetite, abdominal mass or weight loss. Women have an increased risk of lobular breast cancer as well. Is a Adenocarcinoma of stomach (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary diffuse gastric cancer is a rare epithelial tumor of the stomach, characterized by the development of diffuse (signet ring cell) gastric cancer at a young age, associated with germline heterozygous mutations of CDH1, MAP3K6 and CTNNA1 genes. In early stages it presents with non-specific and vague symptoms, in advanced stages it may cause nausea and vomiting, dysphagia, loss of appetite, abdominal mass or weight loss. Women have an increased risk of lobular breast cancer as well. Is a Hereditary cancer-predisposing syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary diffuse gastric cancer is a rare epithelial tumor of the stomach, characterized by the development of diffuse (signet ring cell) gastric cancer at a young age, associated with germline heterozygous mutations of CDH1, MAP3K6 and CTNNA1 genes. In early stages it presents with non-specific and vague symptoms, in advanced stages it may cause nausea and vomiting, dysphagia, loss of appetite, abdominal mass or weight loss. Women have an increased risk of lobular breast cancer as well. Associated morphology Carcinoma, diffuse type (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary diffuse gastric cancer is a rare epithelial tumor of the stomach, characterized by the development of diffuse (signet ring cell) gastric cancer at a young age, associated with germline heterozygous mutations of CDH1, MAP3K6 and CTNNA1 genes. In early stages it presents with non-specific and vague symptoms, in advanced stages it may cause nausea and vomiting, dysphagia, loss of appetite, abdominal mass or weight loss. Women have an increased risk of lobular breast cancer as well. Finding site Stomach structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary diffuse gastric cancer is a rare epithelial tumor of the stomach, characterized by the development of diffuse (signet ring cell) gastric cancer at a young age, associated with germline heterozygous mutations of CDH1, MAP3K6 and CTNNA1 genes. In early stages it presents with non-specific and vague symptoms, in advanced stages it may cause nausea and vomiting, dysphagia, loss of appetite, abdominal mass or weight loss. Women have an increased risk of lobular breast cancer as well. Is a Primary adenocarcinoma of gastrointestinal tract false Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Family history of hereditary diffuse carcinoma of stomach (situation) Associated finding True Hereditary diffuse gastric cancer is a rare epithelial tumor of the stomach, characterized by the development of diffuse (signet ring cell) gastric cancer at a young age, associated with germline heterozygous mutations of CDH1, MAP3K6 and CTNNA1 genes. In early stages it presents with non-specific and vague symptoms, in advanced stages it may cause nausea and vomiting, dysphagia, loss of appetite, abdominal mass or weight loss. Women have an increased risk of lobular breast cancer as well. Inferred relationship Existential restriction modifier (core metadata concept) 1

Reference Sets

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

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