FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

1155732005: Cystic dysplasia of kidney (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
4569809013 Cystic dysplasia of kidney (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4569810015 Cystic renal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4569811016 Cystic dysplasia of kidney en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5907161000241112 dysplasie kystique du rein fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5907171000241116 dysplasie kystique rénale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cystic dysplasia of kidney (disorder) Occurrence Congenital true Inferred relationship Some 2
Cystic dysplasia of kidney (disorder) Finding site Kidney structure true Inferred relationship Some 1
Cystic dysplasia of kidney (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Cystic dysplasia of kidney (disorder) Associated morphology Dysplasia true Inferred relationship Some 1
Cystic dysplasia of kidney (disorder) Finding site Kidney structure true Inferred relationship Some 2
Cystic dysplasia of kidney (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Cystic dysplasia of kidney (disorder) Occurrence Congenital true Inferred relationship Some 1
Cystic dysplasia of kidney (disorder) Is a Renal dysplasia true Inferred relationship Some
Cystic dysplasia of kidney (disorder) Associated morphology Cyst true Inferred relationship Some 2
Cystic dysplasia of kidney (disorder) Is a Congenital renal cyst (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
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 Cystic dysplasia of kidney (disorder) Inferred relationship Some

Reference Sets

GB English

US English

Back to Start