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715561008: 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
3303027010 Hereditary papillary renal cell carcinoma (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
3303029013 A familial predisposition for developing bilateral and multifocal type 1 papillary renal carcinoma. Transmitted as an autosomal dominant trait with reduced penetrance, the syndrome is associated with germline mutations in the MET proto-oncogene (7q31). en Definition Active Entire term case sensitive (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
3396071001000113 Nierenzellkarzinom, papilläres, familiäres de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
878601000172113 HPRCC - hereditary papillary renal cell carcinoma fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
896211000172117 cancer papillaire rénal héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
878601000172113 HPRCC - hereditary papillary renal cell carcinoma fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
896211000172117 cancer papillaire rénal héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3396071001000113 Nierenzellkarzinom, papilläres, familiäres 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
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). Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
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). Is a Familial neoplastic disease false Inferred relationship Existential restriction modifier (core metadata concept)
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). Is a Primary malignant neoplasm of kidney false Inferred relationship Existential restriction modifier (core metadata concept)
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). Is a Malignant adenomatous neoplasm false Inferred relationship Existential restriction modifier (core metadata concept)
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). Is a Hereditary nephropathy (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
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). Associated morphology Papillary adenocarcinoma false Inferred relationship Existential restriction modifier (core metadata concept) 1
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). Finding site Kidney structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
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). Is a Hereditary cancer-predisposing syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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