1259808003: Primary solid neoplasm with neurotrophic receptor tyrosine kinase gene fusion (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Solid neoplasm with neurotrophic receptor tyrosine kinase gene fusion\Primary solid neoplasm with neurotrophic receptor tyrosine kinase gene fusion
• \Neoplasm and/or hamartoma\Neoplastic disease\Malignant neoplastic disease\...
• \Solid neoplasm with neurotrophic receptor tyrosine kinase gene fusion\Primary solid neoplasm with neurotrophic receptor tyrosine kinase gene fusion
• \Primary malignant neoplasm\Primary solid neoplasm with neurotrophic receptor tyrosine kinase gene fusion

Status: current, Defined. Date: 31-Dec 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5157943010	Primary solid tumor with NTRK gene fusion	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
5157944016	Primary solid tumour with neurotrophic receptor tyrosine kinase	en	Synonym	Active	Case insensitive	SNOMED CT core
5157945015	Primary solid neoplasm with neurotrophic receptor tyrosine kinase gene fusion	en	Synonym	Active	Case insensitive	SNOMED CT core
5157946019	Primary solid neoplasm with neurotrophic receptor tyrosine kinase gene fusion (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
5157947011	Primary solid tumour with NTRK gene fusion	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
5157948018	Primary solid tumor with neurotrophic receptor tyrosine kinase	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Australian dialect reference set

Neoplasm and/or hamartoma reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

Back to Start