737562008: Multicystic renal dysplasia (disorder)

Descriptions:

Id Description Lang Type Status Case? Module

3528306010 Multicystic renal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3528307018 Multicystic dysplastic kidney en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3528308011 Multicystic renal dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3528309015 MCKD - Multicystic kidney disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

5403899019 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Bilateral multicystic renal dysplasia (disorder)	Is a	True	Multicystic renal dysplasia	Inferred relationship	Some
Unilateral multicystic renal dysplasia	Is a	True	Multicystic renal dysplasia	Inferred relationship	Some

Reference Sets

Id	Description	Lang	Type	Status	Case?	Module
3528306010	Multicystic renal dysplasia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3528307018	Multicystic dysplastic kidney	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3528308011	Multicystic renal dysplasia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3528309015	MCKD - Multicystic kidney disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5403899019	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.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core