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722721004: familiair hemolytisch-uremisch syndroom (aandoening)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3333162015 Familial haemolytic uraemic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3333164019 Familial hemolytic uremic syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3333165018 Familial hemolytic uremic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
8391671000146119 familiair hemolytisch-uremisch syndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8391681000146117 familiair hemolytisch-uremisch syndroom (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8391691000146115 familiair HUS nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3333166017 Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3333167014 Hemolytic uremic syndrome with either a family history of haemolytic uremic syndrome or a genetic mutation known to cause haemolytic uremic syndrome, or both. en Definition Inactive Entire term case sensitive (core metadata concept) SNOMED CT core
4544148017 Hemolytic uremic syndrome with either a family history of hemolytic uremic syndrome or a genetic mutation known to cause hemolytic uremic syndrome, or both. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial haemolytic uraemic syndrome Is a Familial disease true Inferred relationship Some
Familial haemolytic uraemic syndrome Is a Congenital hemolytic uremic syndrome (disorder) false Inferred relationship Some
Familial haemolytic uraemic syndrome Occurrence Congenital false Inferred relationship Some
Familial haemolytic uraemic syndrome Clinical course Sudden onset AND/OR short duration (qualifier value) true Inferred relationship Some 1
Familial haemolytic uraemic syndrome Finding site Erythrocyte false Inferred relationship Some
Familial haemolytic uraemic syndrome Finding site Kidney structure true Inferred relationship Some 7
Familial haemolytic uraemic syndrome Has definitional manifestation erytropenie (bevinding) false Inferred relationship Some
Familial haemolytic uraemic syndrome Has definitional manifestation Hemolysis false Inferred relationship Some
Familial haemolytic uraemic syndrome Has interpretation Below reference range true Inferred relationship Some 10
Familial haemolytic uraemic syndrome Interprets Measurement of total haemoglobin concentration true Inferred relationship Some 10
Familial haemolytic uraemic syndrome Has interpretation Below reference range true Inferred relationship Some 11
Familial haemolytic uraemic syndrome Interprets Red blood cell count true Inferred relationship Some 11
Familial haemolytic uraemic syndrome Associated morphology Schistocyte false Inferred relationship Some 12
Familial haemolytic uraemic syndrome Finding site Hematopoietic system structure false Inferred relationship Some 12
Familial haemolytic uraemic syndrome Interprets Erythrocyte destruction false Inferred relationship Some
Familial haemolytic uraemic syndrome Is a Hemolytic uremic syndrome true Inferred relationship Some
Familial haemolytic uraemic syndrome Associated morphology Schistocyte true Inferred relationship Some 4
Familial haemolytic uraemic syndrome Has interpretation Below reference range true Inferred relationship Some 3
Familial haemolytic uraemic syndrome Interprets Platelet count true Inferred relationship Some 3
Familial haemolytic uraemic syndrome Interprets Measurement of renal function false Inferred relationship Some 2
Familial haemolytic uraemic syndrome Has interpretation Impaired false Inferred relationship Some 2
Familial haemolytic uraemic syndrome Interprets Hemolysis (observable entity) true Inferred relationship Some 5
Familial haemolytic uraemic syndrome Finding site Erythrocyte false Inferred relationship Some 6
Familial haemolytic uraemic syndrome Has interpretation Present true Inferred relationship Some 5
Familial haemolytic uraemic syndrome Occurrence Period of life beginning after birth and ending before death (qualifier value) false Inferred relationship Some 6
Familial haemolytic uraemic syndrome Finding site Erythrocyte true Inferred relationship Some 8
Familial haemolytic uraemic syndrome Interprets Renal function true Inferred relationship Some 9
Familial haemolytic uraemic syndrome Has interpretation Impaired true Inferred relationship Some 9
Familial haemolytic uraemic syndrome Finding site Structure of capillary blood vessel true Inferred relationship Some 2
Familial haemolytic uraemic syndrome Associated morphology Microthrombus (morphologic abnormality) true Inferred relationship Some 2
Familial haemolytic uraemic syndrome Finding site Structure of arteriole true Inferred relationship Some 6
Familial haemolytic uraemic syndrome Associated morphology Microthrombus (morphologic abnormality) true Inferred relationship Some 6
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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