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765330003: autosomaal dominante polycysteuze nierziekte (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
3657944013 Autosomal dominant polycystic kidney disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3657945014 Autosomal dominant polycystic kidney disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3657946010 ADPKD - autosomal dominant polycystic kidney disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6352911000146113 autosomaal dominante polycysteuze nierziekte nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6352921000146115 autosomaal dominante cystenieren nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6352931000146118 ADCN nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6352941000146114 autosomaal dominante polycysteuze nierziekte (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6352951000146112 ADPKD nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3657947018 Inherited disease with characteristics of the development of cysts in the kidneys. The disease rarely causes any noticeable problems until the cysts grow large enough to affect renal function, usually between 30 and 60 years of age. Less commonly, children or older people may have noticeable symptoms. Two different genes are known to cause this disease PKD1 and PKD2. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
10388751000146111 Autosomaal dominante polycysteuze nierziekte; vorm van cystenieren die autosomaal dominant overerft, dat wil zeggen dat iemand 50% kans heeft dat hij de aanleg erft indien een van de ouders de ziekte heeft. nl Definition Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant polycystic kidney disease (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant polycystic kidney disease (disorder) Finding site Kidney structure true Inferred relationship Some 1
Autosomal dominant polycystic kidney disease (disorder) Is a Congenital cystic kidney disease true Inferred relationship Some
Autosomal dominant polycystic kidney disease (disorder) Occurrence Congenital true Inferred relationship Some 1
Autosomal dominant polycystic kidney disease (disorder) Associated morphology Polycystic change true Inferred relationship Some 1
Autosomal dominant polycystic kidney disease (disorder) Is a Hereditary nephropathy (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Adult type polycystic kidney disease type 2 (disorder) Is a True Autosomal dominant polycystic kidney disease (disorder) Inferred relationship Some
Adult type polycystic kidney disease type 1 (disorder) Is a True Autosomal dominant polycystic kidney disease (disorder) Inferred relationship Some
Autosomal dominant polycystic kidney disease in childhood Is a True Autosomal dominant polycystic kidney disease (disorder) Inferred relationship Some
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis (disorder) Is a True Autosomal dominant polycystic kidney disease (disorder) Inferred relationship Some
Multinodular goiter, cystic kidney, polydactyly syndrome (disorder) Is a True Autosomal dominant polycystic kidney disease (disorder) Inferred relationship Some
Adult type polycystic kidney disease Is a False Autosomal dominant polycystic kidney disease (disorder) Inferred relationship Some

This concept is not in any reference sets

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