715561008: Hereditary papillary renal cell carcinoma (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\Genetic disease\Hereditary disease\...
• \Hereditary cancer-predisposing syndrome\Hereditary papillary renal cell carcinoma (disorder)
• \Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary papillary renal cell carcinoma (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
3303027010	Hereditary papillary renal cell carcinoma (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3303028017	Hereditary papillary renal cell carcinoma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5400964018	A rare familial renal cancer syndrome characterized by a predisposition for developing bilateral and multifocal classic type papillary renal cell carcinomas (formerly known as type 1 papillary renal cell carcinoma until the 2022 WHO classification of renal tumors).	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5400965017	A rare familial renal cancer syndrome characterised by a predisposition for developing bilateral and multifocal classic type papillary renal cell carcinomas (formerly known as type 1 papillary renal cell carcinoma until the 2022 WHO classification of renal tumours).	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

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

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