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1264001009: De novo thrombotic microangiopathy following transplant of kidney (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5170842015 De novo thrombotic microangiopathy after kidney transplantation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5170843013 De novo thrombotic microangiopathy following transplant of kidney (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5170844019 De novo thrombotic microangiopathy following transplant of kidney en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5170851011 De novo thrombotic microangiopathy after renal transplant en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5400457010 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400458017 A rare renal disease characterised 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 haemolytic anaemia, and acute kidney injury. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5170842015 De novo thrombotic microangiopathy after kidney transplantation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5170843013 De novo thrombotic microangiopathy following transplant of kidney (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5170844019 De novo thrombotic microangiopathy following transplant of kidney en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5170851011 De novo thrombotic microangiopathy after renal transplant en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5170849012 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5170850012 A rare renal disease characterised 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 haemolytic anaemia and acute kidney injury. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400457010 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400458017 A rare renal disease characterised 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 haemolytic anaemia, and acute kidney injury. 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
De novo thrombotic microangiopathy following transplant of kidney Is a Thrombotic microangiopathy true Inferred relationship Existential restriction modifier (core metadata concept)
De novo thrombotic microangiopathy following transplant of kidney Is a Postoperative complication (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
De novo thrombotic microangiopathy following transplant of kidney Is a Disorder related to renal transplantation (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
De novo thrombotic microangiopathy following transplant of kidney Is a Arterial complication of procedure true Inferred relationship Existential restriction modifier (core metadata concept)
De novo thrombotic microangiopathy following transplant of kidney After Transplant of kidney true Inferred relationship Existential restriction modifier (core metadata concept) 3
De novo thrombotic microangiopathy following transplant of kidney Finding site Structure of capillary blood vessel true Inferred relationship Existential restriction modifier (core metadata concept) 1
De novo thrombotic microangiopathy following transplant of kidney Associated morphology Microthrombus (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
De novo thrombotic microangiopathy following transplant of kidney Finding site Structure of arteriole (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
De novo thrombotic microangiopathy following transplant of kidney Associated morphology Microthrombus (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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