765330003: Autosomal dominant polycystic kidney disease (disorder)

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

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

873291000172114 polykystose rénale autosomique dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

889621000172116 ADPKD - autosomal dominant polycystic kidney disease fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)

949001000172118 autosomaal dominante polycystische nierziekte nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

949281000172115 ADPKD - autosomal dominant polycystic kidney disease nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)

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

Reference Sets

Belgian GP subset (foundation metadata concept)

Belgian subset for medical problems in patient health records

Back to Start

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
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
873291000172114	polykystose rénale autosomique dominante	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
889621000172116	ADPKD - autosomal dominant polycystic kidney disease	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)
949001000172118	autosomaal dominante polycystische nierziekte	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
949281000172115	ADPKD - autosomal dominant polycystic kidney disease	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)