715561008: hereditair papillair niercelcarcinoom (aandoening)

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

6361131000146116 hereditair papillair niercelcarcinoom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6361141000146112 erfelijk papillair niercarcinoom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6361151000146110 hereditair papillair NCC nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6361161000146113 hereditair papillair niercelcarcinoom (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

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

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary papillary renal cell carcinoma (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Hereditary papillary renal cell carcinoma (disorder)	Is a	Familial neoplastic disease	false	Inferred relationship	Some
Hereditary papillary renal cell carcinoma (disorder)	Is a	Primary malignant neoplasm of kidney	false	Inferred relationship	Some
Hereditary papillary renal cell carcinoma (disorder)	Is a	Malignant adenomatous neoplasm (disorder)	false	Inferred relationship	Some
Hereditary papillary renal cell carcinoma (disorder)	Is a	Hereditary nephropathy (disorder)	false	Inferred relationship	Some
Hereditary papillary renal cell carcinoma (disorder)	Associated morphology	Papillary adenocarcinoma	false	Inferred relationship	Some	1
Hereditary papillary renal cell carcinoma (disorder)	Finding site	Kidney structure	false	Inferred relationship	Some	1
Hereditary papillary renal cell carcinoma (disorder)	Is a	Hereditary cancer-predisposing syndrome	true	Inferred relationship	Some

Inbound Relationships

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This concept is not in any reference sets