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254914004: Neoplasm of parenchyma of kidney (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
379795012 Tumour of kidney parenchyma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
379796013 Tumor of kidney parenchyma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3991221015 Neoplasm of parenchyma of kidney (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3991222010 Neoplasm of parenchyma of kidney en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5922421000241117 néoplasme du parenchyme rénal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5922431000241115 tumeur du parenchyme rénal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

34 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neoplasm of parenchyma of kidney (disorder) Is a Neoplasm of kidney true Inferred relationship Some
Neoplasm of parenchyma of kidney (disorder) Associated morphology Neoplasm false Inferred relationship Some 1
Neoplasm of parenchyma of kidney (disorder) Finding site Kidney structure false Inferred relationship Some 1
Neoplasm of parenchyma of kidney (disorder) Pathological process Neoplastic process false Inferred relationship Some
Neoplasm of parenchyma of kidney (disorder) Finding site Anatomical structure false Inferred relationship Some 1
Neoplasm of parenchyma of kidney (disorder) Associated morphology Neoplasm true Inferred relationship Some 1
Neoplasm of parenchyma of kidney (disorder) Finding site Kidney structure false Inferred relationship Some 1
Neoplasm of parenchyma of kidney (disorder) Is a Disorder of renal parenchyma (disorder) true Inferred relationship Some
Neoplasm of parenchyma of kidney (disorder) Finding site Structure of parenchyma of kidney true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Papillary thyroid carcinoma with renal papillary neoplasia (disorder) Is a False Neoplasm of parenchyma of kidney (disorder) Inferred relationship Some
Malignant neoplasm of kidney parenchyma Is a True Neoplasm of parenchyma of kidney (disorder) Inferred relationship Some
Mesoblastic nephroma Is a True Neoplasm of parenchyma of kidney (disorder) Inferred relationship Some
Benign neoplasm of renal parenchyma Is a True Neoplasm of parenchyma of kidney (disorder) Inferred relationship Some
A rare, secondary glomerular disease characterized by proteinuria, dysproteinemias, nephrotic syndrome, and nodular glomerulopathy leading to renal failure, with or without extra-renal manifestations. The renal biopsy shows typical deposits of monoclonal immunoglobulins that do not show a fibrillar organization and are negative for Congo red staining. Associated signs and symptoms depend on the involvement of other organs, liver, heart, nerve fibers, gastrointestinal tract, or skin. Is a True Neoplasm of parenchyma of kidney (disorder) Inferred relationship Some
Cystic partially differentiated nephroblastoma of kidney Is a True Neoplasm of parenchyma of kidney (disorder) Inferred relationship Some
Solitary fibrous tumor of kidney Is a True Neoplasm of parenchyma of kidney (disorder) Inferred relationship Some
Clear cell papillary renal cell carcinoma is a rare, indolent subtype of clear cell renal carcinoma, arising from epithelial cells in the renal cortex. It most frequently manifests with a well-circumscribed, well-encapsulated, unicentric, unilateral, small tumour that typically does not metastasize. Clinically it can present with flank or abdominal pain or haematuria, although most patients are usually asymptomatic at the time of diagnosis. Bilateral and/or multifocal presentation should raise the suspicion of von Hippel-Lindau syndrome. Is a True Neoplasm of parenchyma of kidney (disorder) Inferred relationship Some

This concept is not in any reference sets

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