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737562008: multicysteuze dysplasie van nier (aandoening)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

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
8262341000146116 multicysteuze dysplasie van nier nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8262361000146115 multicysteuze dysplasie van nier (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8283191000146116 multicysteuze dysplastische nier nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8283201000146119 multicysteuze renale dysplasie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8283211000146117 multicysteuze nierdysplasie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3528310013 A congenital anomaly of the kidney and urinary tract in which one or both kidneys are large, distended by multiple cysts, and non-functional. Global prevalence is not known, but the unilateral form is the most frequent. The disorder frequently presents antenatally at routine ultrasound scan. Bilateral disease is considered a lethal entity and most pregnancies are terminated. The disorder results from disrupted nephrogenesis but the exact pathogenic mechanism is still unknown. Mutations in the HNF1B gene (17q12) are strongly associated with the development of this disease. Most cases are sporadic. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

2 descendants. Search Descendants:

Expanded Value Set

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

This concept is not in any reference sets

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