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765330003: Autosomal dominant polycystic kidney disease (disorder)


Status: current, Defined. 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 Case insensitive SNOMED CT core
3657945014 Autosomal dominant polycystic kidney disease en Synonym Active Case insensitive SNOMED CT core
3657946010 ADPKD - autosomal dominant polycystic kidney disease en Synonym Active Case sensitive 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 Case sensitive SNOMED CT core


5 descendants. Search Descendants:

Expanded Value Set


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

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

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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