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268234004: Fibrocystic 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
400871016 Fibrocystic kidney disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
660950011 Fibrocystic kidney disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5107901000241113 maladie rénale fibrokystique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fibrocystic kidney disease Is a Congenital cystic kidney disease false Inferred relationship Some
Fibrocystic kidney disease Associated morphology Fibrocysticystic change (morphologic abnormality) false Inferred relationship Some 1
Fibrocystic kidney disease Occurrence Congenital false Inferred relationship Some
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 1
Fibrocystic kidney disease 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
Fibrocystic kidney disease Associated morphology anomalie congénitale false Inferred relationship Some 1
Fibrocystic kidney disease Course Multiple superficial injuries of lower leg false Inferred relationship Some
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 1
Fibrocystic kidney disease Associated morphology Fibrocystic change false Inferred relationship Some 2
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 1
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 1
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 1
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 1
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 1
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 1
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
Fibrocystic kidney disease Finding site Kidney structure true Inferred relationship Some 1
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
Fibrocystic kidney disease Associated morphology Polycystic change false Inferred relationship Some 2
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
Fibrocystic kidney disease Occurrence Congenital false Inferred relationship Some 3
Fibrocystic kidney disease Associated morphology anomalie du développement false Inferred relationship Some 3
Fibrocystic kidney disease Finding site Kidney structure false Inferred relationship Some 3
Fibrocystic kidney disease Associated morphology Polycystic change false Inferred relationship Some 1
Fibrocystic kidney disease Occurrence Congenital true Inferred relationship Some 1
Fibrocystic kidney disease Associated morphology Fibrocystic change true Inferred relationship Some 1
Fibrocystic kidney disease Is a Congenital renal cyst (disorder) true Inferred relationship Some
Fibrocystic kidney disease Is a Renal fibrosis true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
A rare ciliopathy characterized by the association of nephronophthisis and liver fibrosis. Renal manifestations include chronic renal failure, polyuria, polydipsia, anemia, as well as increased echogenicity on renal ultrasound and interstitial fibrosis and tubular dilation on biopsy. Hepatic involvement manifests as hepatosplenomegaly with extensive fibrosis, destruction of the bile ducts, and cholestasis. Mild psychomotor retardation and ocular symptoms, such as strabismus, nystagmus, retinal degeneration, and anisocoria, have been reported in some patients. Is a True Fibrocystic kidney disease Inferred relationship Some

This concept is not in any reference sets

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