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253883006: Multiple renal cysts (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
377986015 Multiple renal cysts en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
644699011 Multiple renal cysts (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1844481000195116 cisti renali multiple it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3389985014 kystes rénaux multiples fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Multiple renal cysts Is a maladie kystique du rein false Inferred relationship Some
Multiple renal cysts Finding site Kidney structure false Inferred relationship Some
Multiple renal cysts Is a Cyst of kidney (disorder) true Inferred relationship Some
Multiple renal cysts Associated morphology Multiple cysts true Inferred relationship Some 1
Multiple renal cysts Finding site Kidney structure true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Multiple acquired kidney cysts (disorder) Is a True Multiple renal cysts Inferred relationship Some
A rare congenital anomaly of the kidney and urinary tract (CAKUT) in which one or both kidneys (unilateral or bilateral MCDK respectively) are large, distended by multiple cysts, and non-functional. Unilateral MCDK is typically asymptomatic if the other kidney is fully functional but may occasionally present with abdominal obstructive signs when the cysts become too large. Bilateral MCDK is considered a lethal entity and neonates present with features of the Potter sequence, severe pulmonary hypoplasia and severe renal failure, and generally die shortly after birth. Is a True Multiple renal cysts Inferred relationship Some

This concept is not in any reference sets

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