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126729006: Thrombotic microangiopathy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
135665013 Thrombotic microangiopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
730729015 Thrombotic microangiopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4130911000005115 trombotisk mikroangiopati da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


21 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Thrombotic microangiopathy Is a Thrombotic disorder false Inferred relationship Some
Thrombotic microangiopathy Is a Microangiopathy false Inferred relationship Some
Thrombotic microangiopathy Finding site Blood vessel structure (body structure) false Inferred relationship Some 2
Thrombotic microangiopathy Associated morphology Thrombus false Inferred relationship Some 2
Thrombotic microangiopathy Is a Disorder of capillaries (disorder) false Inferred relationship Some
Thrombotic microangiopathy Finding site Structure of capillary blood vessel false Inferred relationship Some 1
Thrombotic microangiopathy Is a Capillary thrombosis true Inferred relationship Some
Thrombotic microangiopathy Associated morphology Thrombus (morphologic abnormality) false Inferred relationship Some 1
Thrombotic microangiopathy Finding site Structure of capillary blood vessel true Inferred relationship Some 1
Thrombotic microangiopathy Associated morphology Thrombus (morphologic abnormality) false Inferred relationship Some 1
Thrombotic microangiopathy Is a Arterial thrombosis true Inferred relationship Some
Thrombotic microangiopathy Is a Disorder of arteriole true Inferred relationship Some
Thrombotic microangiopathy Associated morphology Microthrombus (morphologic abnormality) true Inferred relationship Some 1
Thrombotic microangiopathy Finding site Structure of arteriole true Inferred relationship Some 2
Thrombotic microangiopathy Associated morphology Microthrombus (morphologic abnormality) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Hemolytic uremic syndrome Is a False Thrombotic microangiopathy Inferred relationship Some
Thrombotic microangiopathy NOS Is a False Thrombotic microangiopathy Inferred relationship Some
Thrombotic thrombocytopenic purpura Is a True Thrombotic microangiopathy Inferred relationship Some
Upshaw-Schulman syndrome (disorder) Is a False Thrombotic microangiopathy Inferred relationship Some
Acute intravascular thrombotic microangiopathy Is a True Thrombotic microangiopathy Inferred relationship Some
Chronic thrombotic microangiopathy Is a True Thrombotic microangiopathy Inferred relationship Some
A rare renal disease characterized by thrombotic microangiopathy developing de novo in kidney transplant recipients with no evidence of occurrence of the disease prior to transplantation. Precipitating factors include antibody-mediated rejection, immunosuppressive medication, viral infections, and genetic abnormalities in the complement cascade, among others. The condition most commonly occurs within the first 3-6 months post-transplantation. Clinical presentation is highly variable and ranges from a limited form confined to the kidney with relatively good prognosis to a systemic variant consisting of the classic triad of thrombocytopenia, microangiopathic hemolytic anemia, and acute kidney injury. Is a True Thrombotic microangiopathy Inferred relationship Some
Thrombotic microangiopathy following hemopoietic stem cell transplant (disorder) Is a True Thrombotic microangiopathy Inferred relationship Some

This concept is not in any reference sets

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