FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

253880009: Autosomal dominant polycystic kidney disease in childhood (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
377982018 Autosomal dominant polycystic kidney disease in childhood en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
644695017 Autosomal dominant polycystic kidney disease in childhood (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5079711000241115 polykystose rénale autosomique dominante de l'enfant fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant polycystic kidney disease in childhood Is a polykystose rénale autosomique dominante false Inferred relationship Some
Autosomal dominant polycystic kidney disease in childhood Associated morphology anomalie congénitale false Inferred relationship Some 1
Autosomal dominant polycystic kidney disease in childhood 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
Autosomal dominant polycystic kidney disease in childhood Occurrence Congenital false Inferred relationship Some
Autosomal dominant polycystic kidney disease in childhood Finding site Kidney structure false Inferred relationship Some 1
Autosomal dominant polycystic kidney disease in childhood Associated morphology Fibrocysticystic change (morphologic abnormality) false Inferred relationship Some 1
Autosomal dominant polycystic kidney disease in childhood Course Multiple superficial injuries of lower leg false Inferred relationship Some
Autosomal dominant polycystic kidney disease in childhood Finding site Kidney structure false Inferred relationship Some 2
Autosomal dominant polycystic kidney disease in childhood Associated morphology Fibrocystic change false Inferred relationship Some 2
Autosomal dominant polycystic kidney disease in childhood Finding site Kidney structure false Inferred relationship Some 2
Autosomal dominant polycystic kidney disease in childhood Finding site Kidney structure false Inferred relationship Some 1
Autosomal dominant polycystic kidney disease in childhood Finding site Kidney structure false Inferred relationship Some 2
Autosomal dominant polycystic kidney disease in childhood Finding site Kidney structure false Inferred relationship Some 1
Autosomal dominant polycystic kidney disease in childhood Finding site Kidney structure false Inferred relationship Some 1
Autosomal dominant polycystic kidney disease in childhood Finding site Kidney structure false Inferred relationship Some 2
Autosomal dominant polycystic kidney disease in childhood Finding site Kidney structure false Inferred relationship Some 1
Autosomal dominant polycystic kidney disease in childhood Finding site Kidney structure false Inferred relationship Some 2
Autosomal dominant polycystic kidney disease in childhood Finding site Kidney structure false Inferred relationship Some 1
Autosomal dominant polycystic kidney disease in childhood Finding site Kidney structure false Inferred relationship Some 2
Autosomal dominant polycystic kidney disease in childhood Finding site Kidney structure false Inferred relationship Some 1
Autosomal dominant polycystic kidney disease in childhood Finding site Kidney structure false Inferred relationship Some 2
Autosomal dominant polycystic kidney disease in childhood Finding site Kidney structure true Inferred relationship Some 1
Autosomal dominant polycystic kidney disease in childhood Finding site Kidney structure false Inferred relationship Some 2
Autosomal dominant polycystic kidney disease in childhood Is a A rare, genetic, renal tubular disease characterized by progressive outgrowths of fluid-filled cysts from the renal epithelium, which can manifest with hematuria, urinary tract infections, hypertension, and abdominal or flank pain. The slowly progressive loss of kidney function may evolve to end stage kidney disease (ESKD). true Inferred relationship Some
Autosomal dominant polycystic kidney disease in childhood Associated morphology Polycystic change true Inferred relationship Some 1
Autosomal dominant polycystic kidney disease in childhood Occurrence Congenital true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

Back to Start