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446569001: Microthrombus (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2011. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2880260011 Microthrombus (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2883072012 Microthrombus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Microthrombus (morphologic abnormality) Is a Thrombus (morphologic abnormality) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Thrombotic microangiopathy Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 1
Thrombotic microangiopathy Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 2
Autoimmune thrombotic thrombocytopenic purpura (disorder) Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 10
Autoimmune thrombotic thrombocytopenic purpura (disorder) Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 1
Acquired thrombotic thrombocytopenic purpura (disorder) Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 10
Acquired thrombotic thrombocytopenic purpura (disorder) Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 1
Drug induced thrombotic thrombocytopenic purpura (disorder) Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 1
Drug induced thrombotic thrombocytopenic purpura (disorder) Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 8
Thrombotic thrombocytopenic purpura Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 2
Thrombotic thrombocytopenic purpura Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 6
Chronic thrombotic microangiopathy Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 1
Chronic thrombotic microangiopathy Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 3
Acute intravascular thrombotic microangiopathy Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 1
Acute intravascular thrombotic microangiopathy Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 3
Upshaw-Schulman syndrome (disorder) Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 9
Upshaw-Schulman syndrome (disorder) Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 10
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. Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 1
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. Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 2
Thrombotic microangiopathy following hemopoietic stem cell transplant (disorder) Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 1
Thrombotic microangiopathy following hemopoietic stem cell transplant (disorder) Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 2
Hemolytic uremic syndrome, adult type Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 10
Hemolytic uremic syndrome, adult type Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 11
Hemolytic uremic syndrome of childhood Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 11
Hemolytic uremic syndrome of childhood Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 12
Diarrhea-associated hemolytic uremic syndrome (disorder) Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 12
Diarrhea-associated hemolytic uremic syndrome (disorder) Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 13
Diarrhea-negative hemolytic uremic syndrome (disorder) Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 10
Diarrhea-negative hemolytic uremic syndrome (disorder) Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 11
Atypical haemolytic uraemic syndrome Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 11
Atypical haemolytic uraemic syndrome Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 12
Congenital hemolytic uremic syndrome (disorder) Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 4
Congenital hemolytic uremic syndrome (disorder) Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 11
Hemolytic uremic syndrome Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 10
Hemolytic uremic syndrome Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 11
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 2
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 6
A rare genetic hemolytic uremic syndrome (HUS) characterized by infantile onset of relapsing episodes of microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. The episodes are often preceded by viral infections. Affected individuals typically present persistent hypertension, hematuria, and proteinuria (sometimes in the nephrotic range) and develop chronic kidney disease with age. Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 10
A rare genetic hemolytic uremic syndrome (HUS) characterized by infantile onset of relapsing episodes of microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. The episodes are often preceded by viral infections. Affected individuals typically present persistent hypertension, hematuria, and proteinuria (sometimes in the nephrotic range) and develop chronic kidney disease with age. Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 11
A rare type of hemolytic uremic syndrome (HUS) characterized by the triad of hemolytic anemia due to generalized thrombotic microangiopathy, thrombocytopenia, and acute kidney injury, and most commonly occurring after acute gastroenteritis due to Shiga toxin-producing enterohemorrhagic Escherichia coli or Shigella dysenteriae. Other infectious causes of HUS include Streptococcus pneumoniae, HIV, Mycoplasma pneumoniae, Histoplasmosis, and Coxsackie virus. Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 11
A rare type of hemolytic uremic syndrome (HUS) characterized by the triad of hemolytic anemia due to generalized thrombotic microangiopathy, thrombocytopenia, and acute kidney injury, and most commonly occurring after acute gastroenteritis due to Shiga toxin-producing enterohemorrhagic Escherichia coli or Shigella dysenteriae. Other infectious causes of HUS include Streptococcus pneumoniae, HIV, Mycoplasma pneumoniae, Histoplasmosis, and Coxsackie virus. Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 12
Atypical haemolytic uraemic syndrome with complement gene abnormality Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 13
Atypical haemolytic uraemic syndrome with complement gene abnormality Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 14
Atypical haemolytic uraemic syndrome with anti-factor H antibodies Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 13
Atypical haemolytic uraemic syndrome with anti-factor H antibodies Associated morphology True Microthrombus (morphologic abnormality) Inferred relationship Some 14

This concept is not in any reference sets

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