FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

766980008: carcinome épidermoïde de l'estomac (trouble)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3663552019 Squamous cell carcinoma of stomach en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3663553012 Gastric squamous cell carcinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3663554018 Squamous cell carcinoma of stomach (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
768721000241114 carcinome épidermoïde de l'estomac (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
879791000172116 carcinome épidermoïde gastrique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
913161000172112 carcinome épidermoïde de l'estomac fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3663555017 A rare epithelial tumor of the stomach, defined histopathologically as keratinizing cell masses with pearl formation, mosaic pattern of cell arrangement, intercellular bridges and high concentrations of sulphydryl or disulphide bonds, arising directly from gastric mucosa, without esophageal involvement. It is characterized by preferential location in the upper third of the stomach, high probability of lympho vascular and serosal invasion and late onset of clinical symptoms associated with poor prognosis including nonspecific symptoms of abdominal pain, dysphagia, vomiting, melena or hematochezia, hematemesis and weight loss. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3663556016 A rare epithelial tumour of the stomach, defined histopathologically as keratinising cell masses with pearl formation, mosaic pattern of cell arrangement, intercellular bridges and high concentrations of sulphydryl or disulphide bonds, arising directly from gastric mucosa, without oesophageal involvement. It is characterised by preferential location in the upper third of the stomach, high probability of lympho vascular and serosal invasion and late onset of clinical symptoms associated with poor prognosis including nonspecific symptoms of abdominal pain, dysphagia, vomiting, melaena or haematochezia, haematemesis and weight loss. 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
Squamous cell carcinoma of stomach morphologie associée (attribut) Squamous cell carcinoma (morphologic abnormality) true Inferred relationship Some 1
Squamous cell carcinoma of stomach est un(e) (attribut) Primary malignant neoplasm of stomach (disorder) true Inferred relationship Some
Squamous cell carcinoma of stomach localisation d'une constatation (attribut) structure de l'estomac true Inferred relationship Some 1
Squamous cell carcinoma of stomach est un(e) (attribut) Malignant epithelial neoplasm (disorder) true Inferred relationship Some
Squamous cell carcinoma of stomach morphologie associée (attribut) Malignant squamous tumor, primary (morphologic abnormality) false Inferred relationship Some 1
Squamous cell carcinoma of stomach est un(e) (attribut) carcinome épidermoïde true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start