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369071000119105: Congenital renal cyst (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3005282014 Congenital renal cyst (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3005333012 Congenital renal cyst en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

27 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital renal cyst (disorder) Is a Cyst of abdomen (disorder) false Inferred relationship Some
Congenital renal cyst (disorder) Is a Congenital disease true Inferred relationship Some
Congenital renal cyst (disorder) Is a Kidney disease false Inferred relationship Some
Congenital renal cyst (disorder) Is a Renal mass false Inferred relationship Some
Congenital renal cyst (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital renal cyst (disorder) Associated morphology Cyst true Inferred relationship Some 1
Congenital renal cyst (disorder) Finding site Kidney structure true Inferred relationship Some 1
Congenital renal cyst (disorder) Is a Cyst of kidney (disorder) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital hemorrhagic renal cyst (disorder) Is a True Congenital renal cyst (disorder) Inferred relationship Some
Congenital cystic kidney disease Is a True Congenital renal cyst (disorder) 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 False Congenital renal cyst (disorder) Inferred relationship Some
A rare syndromic intellectual disability characterised by early developmental delay with failure to thrive, intellectual disability, congenital hepatic fibrosis, renal cystic dysplasia, and dysmorphic facial features (bilateral ptosis, anteverted nostrils, high arched palate, and micrognathia). Variable additional features have been reported, including cerebellar anomalies, postaxial polydactyly, syndactyly, genital anomalies, tachypnoea. There have been no further descriptions in the literature since 1987. Is a False Congenital renal cyst (disorder) Inferred relationship Some
Congenital single renal cyst (disorder) Is a True Congenital renal cyst (disorder) Inferred relationship Some
Fibrocystic kidney disease Is a True Congenital renal cyst (disorder) Inferred relationship Some
Cystic dysplasia of kidney (disorder) Is a True Congenital renal cyst (disorder) Inferred relationship Some

This concept is not in any reference sets

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