715561008: Hereditary papillary renal cell carcinoma (disorder)

• SNOMED CT Concept\Clinical finding\Disease\Genetic disease\Hereditary disease\...
• \Hereditary neoplastic syndrome\Hereditary papillary renal cell carcinoma
• \Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary papillary renal cell carcinoma

Status: current, Primitive. 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	Case insensitive	SNOMED CT core
3303028017	Hereditary papillary renal cell carcinoma	en	Synonym	Active	Case insensitive	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	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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