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1144764001: Malignant neoplasm of esophagus with neuregulin 1 gene fusion (disorder)


Status: current, Primitive. Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4543139018 Malignant tumor of esophagus with NRG1 fusion en Synonym Active Initial character case insensitive SNOMED CT core
4543140016 Malignant tumour of oesophagus with NRG1 fusion en Synonym Active Initial character case insensitive SNOMED CT core
4543141017 Malignant neoplasm of esophagus with neuregulin 1 gene fusion en Synonym Active Case insensitive SNOMED CT core
4543142012 Malignant neoplasm of oesophagus with NRG1 (neuregulin 1) gene fusion en Synonym Active Initial character case insensitive SNOMED CT core
4543143019 Malignant neoplasm of esophagus with neuregulin 1 gene fusion (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4543144013 Malignant neoplasm of esophagus with NRG1 (neuregulin 1) gene fusion en Synonym Active Initial character case insensitive SNOMED CT core
4543145014 Malignant neoplasm of oesophagus with neuregulin 1 gene fusion en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Malignant tumour of oesophagus with NRG1 fusion Is a Genetic disease true Inferred relationship Some
Malignant tumour of oesophagus with NRG1 fusion Is a Malignant tumour of oesophagus true Inferred relationship Some
Malignant tumour of oesophagus with NRG1 fusion Associated morphology Malignant Neoplasm (Morphology) false Inferred relationship Some 1
Malignant tumour of oesophagus with NRG1 fusion Finding site Oesophageal structure true Inferred relationship Some 1
Malignant tumour of oesophagus with NRG1 fusion Associated morphology Malignant neoplasm true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Neoplasm and/or hamartoma reference set

Problem/Diagnosis reference set

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