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204949001: Renal dysplasia (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
314265017 Renal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
314267013 Dysplasia of kidney en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
314268015 Dysplastic kidney en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
590247014 Renal dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1494972011 Congenital renal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
967531000172118 dysplasie rénale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


16 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Renal dysplasia Is a Congenital anomaly of the kidney (disorder) true Inferred relationship Some
Renal dysplasia Finding site Kidney structure true Inferred relationship Some 1
Renal dysplasia Finding site Urinary tract includes entire kidney and the urinary tract proper which relate to the ureter, bladder and urethra. false Inferred relationship Some 9
Renal dysplasia Course Multiple superficial injuries of lower leg false Inferred relationship Some
Renal dysplasia Occurrence Congenital false Inferred relationship Some
Renal dysplasia Associated morphology anomalie congénitale false Inferred relationship Some 2
Renal dysplasia Associated morphology Congenital dysplasia false Inferred relationship Some 1
Renal dysplasia Is a Congenital malformation false Inferred relationship Some
Renal dysplasia Is a Congenital malformation of the urinary system (disorder) false Inferred relationship Some
Renal dysplasia Finding site Kidney structure false Inferred relationship Some 1
Renal dysplasia Associated morphology Congenital dysplasia false Inferred relationship Some 1
Renal dysplasia Occurrence Congenital false Inferred relationship Some 2
Renal dysplasia Associated morphology anomalie du développement false Inferred relationship Some 2
Renal dysplasia Finding site Kidney structure false Inferred relationship Some 2
Renal dysplasia Is a Kidney lesion true Inferred relationship Some
Renal dysplasia Occurrence Congenital false Inferred relationship Some 3
Renal dysplasia Associated morphology Congenital dysplasia false Inferred relationship Some 3
Renal dysplasia Finding site Kidney structure false Inferred relationship Some 3
Renal dysplasia Occurrence Congenital true Inferred relationship Some 1
Renal dysplasia Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Renal dysplasia Associated morphology Dysplasia true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Bilateral renal dysplasia Is a False Renal dysplasia Inferred relationship Some
Unilateral renal dysplasia Is a False Renal dysplasia Inferred relationship Some
Congenital renal dysplasia Is a False Renal dysplasia Inferred relationship Some
Dysplasia of kidney NOS Is a False Renal dysplasia Inferred relationship Some
[EDTA] Congenital renal dysplasia with or without urinary tract malformation associated with renal failure Is a False Renal dysplasia Inferred relationship Some
Unilateral renal dysplasia Associated finding False Renal dysplasia Inferred relationship Some 1
Unilateral renal dysplasia Associated finding False Renal dysplasia Inferred relationship Some 1
Saldino-Mainzer dysplasia Is a True Renal dysplasia Inferred relationship Some
Renal dysplasia co-occurrent with megalocystis and sirenomelia Is a False Renal dysplasia Inferred relationship Some
Ulbright-Hodes syndrome is characterized by renal dysplasia, growth retardation, phocomelia or mesomelia, radiohumeral fusion, rib abnormalities, anomalies of the external genitalia and a Potter-like facies. The syndrome has been described in three infants (one pair of siblings and an unrelated case), all of whom died shortly after birth from respiratory distress resulting from pulmonary hypoplasia and oligohydramnios caused by renal dysplasia. The mode of transmission appears to be autosomal recessive. Is a True Renal dysplasia Inferred relationship Some
Primary renal dysplasia (disorder) Is a True Renal dysplasia Inferred relationship Some
Secondary renal dysplasia (disorder) Is a True Renal dysplasia Inferred relationship Some
This syndrome is characterized by intrauterine growth retardation, renal dysgenesis and a unilobed or absent thymus. Is a True Renal dysplasia Inferred relationship Some
Agenesis of right kidney co-occurrent with congenital dysplasia of left kidney (disorder) Is a False Renal dysplasia Inferred relationship Some
Agenesis of left kidney co-occurrent with congenital dysplasia of right kidney (disorder) Is a False Renal dysplasia Inferred relationship Some
Dysplasia of left kidney Is a True Renal dysplasia Inferred relationship Some
Dysplasia of right kidney Is a True Renal dysplasia Inferred relationship Some
Torticollis-keloids-cryptorchidism-renal dysplasia syndrome is an extremely rare developmental defect during embryogenesis malformation syndrome characterized by congenital muscular torticollis associated with skin anomalies (such as multiple keloids, pigmented nevi, epithelioma), urogenital malformations (including cryptorchidism and hypospadias) and renal dysplasia (e.g. chronic pyelonephritis, renal atrophy). Additional reported features include varicose veins, intellectual disability and musculoskeletal anomalies. Is a True Renal dysplasia 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 Renal dysplasia Inferred relationship Some
Cystic dysplasia of kidney (disorder) Is a True Renal dysplasia Inferred relationship Some

Reference Sets

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