715561008: cancer papillaire rénal héréditaire (trouble)

• SNOMED CT Concept\constatation clinique\Disease\Genetic disease\maladie héréditaire\...
• \syndrome familial avec prédisposition aux cancers (trouble)\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
747871000241114	cancer papillaire rénal héréditaire (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
878601000172113	HPRCC - hereditary papillary renal cell carcinoma	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
896211000172117	cancer papillaire rénal héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation 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

This concept is not in any reference sets

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