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373420004: Upshaw-Schulman syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1198718017 Upshaw-Schulman syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1211899017 Upshaw-Schulman syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1216561016 Familial thrombotic thrombocytopenic purpura / haemolytic uraemic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1218052015 Familial thrombotic thrombocytopenic purpura / hemolytic uremic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1229241011 Familial TTP/HUS en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5150505018 Congenital ADAMTS-13 deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1198718017 Upshaw-Schulman syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1211899017 Upshaw-Schulman syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1216561016 Familial thrombotic thrombocytopenic purpura / haemolytic uraemic syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1216561016 Familial thrombotic thrombocytopenic purpura / haemolytic uraemic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1218052015 Familial thrombotic thrombocytopenic purpura / hemolytic uremic syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1218052015 Familial thrombotic thrombocytopenic purpura / hemolytic uremic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1229241011 Familial TTP/HUS en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5150505018 Congenital ADAMTS-13 deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3442881001000117 Thrombotisch-thrombozytopenische Purpura, kongenitale Form de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5239901000241113 purpura thrombotique thrombocytopénique familial fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5239901000241113 purpura thrombotique thrombocytopénique familial fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3442881001000117 Thrombotisch-thrombozytopenische Purpura, kongenitale Form de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Upshaw-Schulman syndrome (disorder) Is a Microangiopathic hemolytic anemia false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Is a Thrombocytopenic purpura false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Is a Thrombotic microangiopathy false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Associated morphology Purpura false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Finding site Platelet (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Finding site Peripheral vascular system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Finding site Blood vessel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Upshaw-Schulman syndrome (disorder) Associated morphology Thrombus false Inferred relationship Existential restriction modifier (core metadata concept) 1
Upshaw-Schulman syndrome (disorder) Associated morphology Schistocyte false Inferred relationship Existential restriction modifier (core metadata concept) 1
Upshaw-Schulman syndrome (disorder) Finding site Structure of capillary blood vessel false Inferred relationship Existential restriction modifier (core metadata concept) 2
Upshaw-Schulman syndrome (disorder) Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Finding site Entire hematological system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Upshaw-Schulman syndrome (disorder) Has definitional manifestation érythropénie false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Upshaw-Schulman syndrome (disorder) Associated morphology Thrombus (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Upshaw-Schulman syndrome (disorder) Associated morphology Purpura false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Is a Disorder of hematopoietic structure (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Has definitional manifestation Platelet count below reference range (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Has definitional manifestation Hemolysis false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Has definitional manifestation Hemostatic system finding (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Has definitional manifestation purpura false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Finding site Structure of capillary blood vessel false Inferred relationship Existential restriction modifier (core metadata concept) 2
Upshaw-Schulman syndrome (disorder) Associated morphology Schistocyte false Inferred relationship Existential restriction modifier (core metadata concept) 1
Upshaw-Schulman syndrome (disorder) Associated morphology Thrombus (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Upshaw-Schulman syndrome (disorder) Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Upshaw-Schulman syndrome (disorder) Is a Thrombotic thrombocytopenic purpura true Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Is a Hereditary red blood cell disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Is a Inherited platelet disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Associated morphology Schistocyte false Inferred relationship Existential restriction modifier (core metadata concept) 9
Upshaw-Schulman syndrome (disorder) Has interpretation Below reference range false Inferred relationship Existential restriction modifier (core metadata concept) 1
Upshaw-Schulman syndrome (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 3
Upshaw-Schulman syndrome (disorder) Interprets Measurement of total haemoglobin concentration false Inferred relationship Existential restriction modifier (core metadata concept) 3
Upshaw-Schulman syndrome (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 4
Upshaw-Schulman syndrome (disorder) Interprets Red blood cell count false Inferred relationship Existential restriction modifier (core metadata concept) 4
Upshaw-Schulman syndrome (disorder) Interprets Platelet count false Inferred relationship Existential restriction modifier (core metadata concept) 1
Upshaw-Schulman syndrome (disorder) Interprets Erythrocyte destruction false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Occurrence Period of life between birth and death false Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 5
Upshaw-Schulman syndrome (disorder) Associated morphology Purpura false Inferred relationship Existential restriction modifier (core metadata concept) 5
Upshaw-Schulman syndrome (disorder) Is a Hereditary disorder of the integument (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Occurrence Period of life between birth and death false Inferred relationship Existential restriction modifier (core metadata concept) 6
Upshaw-Schulman syndrome (disorder) Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept) 6
Upshaw-Schulman syndrome (disorder) Has interpretation Present (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 7
Upshaw-Schulman syndrome (disorder) Interprets Haemolysis false Inferred relationship Existential restriction modifier (core metadata concept) 7
Upshaw-Schulman syndrome (disorder) Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 8
Upshaw-Schulman syndrome (disorder) Interprets Hemostatic function false Inferred relationship Existential restriction modifier (core metadata concept) 8
Upshaw-Schulman syndrome (disorder) Occurrence Period of life between birth and death false Inferred relationship Existential restriction modifier (core metadata concept) 10
Upshaw-Schulman syndrome (disorder) Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 1
Upshaw-Schulman syndrome (disorder) Interprets Hemostatic function false Inferred relationship Existential restriction modifier (core metadata concept) 1
Upshaw-Schulman syndrome (disorder) Occurrence Period of life between birth and death false Inferred relationship Existential restriction modifier (core metadata concept) 5
Upshaw-Schulman syndrome (disorder) Interprets Platelet count false Inferred relationship Existential restriction modifier (core metadata concept) 8
Upshaw-Schulman syndrome (disorder) Has interpretation Below reference range false Inferred relationship Existential restriction modifier (core metadata concept) 8
Upshaw-Schulman syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Upshaw-Schulman syndrome (disorder) Finding site Erythrocyte true Inferred relationship Existential restriction modifier (core metadata concept) 8
Upshaw-Schulman syndrome (disorder) Associated morphology Schistocyte true Inferred relationship Existential restriction modifier (core metadata concept) 7
Upshaw-Schulman syndrome (disorder) Interprets Hemostatic function true Inferred relationship Existential restriction modifier (core metadata concept) 2
Upshaw-Schulman syndrome (disorder) Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 2
Upshaw-Schulman syndrome (disorder) Interprets Red blood cell count true Inferred relationship Existential restriction modifier (core metadata concept) 3
Upshaw-Schulman syndrome (disorder) Interprets Measurement of total haemoglobin concentration true Inferred relationship Existential restriction modifier (core metadata concept) 4
Upshaw-Schulman syndrome (disorder) Interprets Platelet count true Inferred relationship Existential restriction modifier (core metadata concept) 5
Upshaw-Schulman syndrome (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 5
Upshaw-Schulman syndrome (disorder) Interprets Haemolysis true Inferred relationship Existential restriction modifier (core metadata concept) 6
Upshaw-Schulman syndrome (disorder) Has interpretation Present (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 6
Upshaw-Schulman syndrome (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Upshaw-Schulman syndrome (disorder) Associated morphology Purpura true Inferred relationship Existential restriction modifier (core metadata concept) 1
Upshaw-Schulman syndrome (disorder) Finding site Structure of arteriole (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 9
Upshaw-Schulman syndrome (disorder) Associated morphology Microthrombus (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 9
Upshaw-Schulman syndrome (disorder) Finding site Structure of capillary blood vessel true Inferred relationship Existential restriction modifier (core metadata concept) 10
Upshaw-Schulman syndrome (disorder) Associated morphology Microthrombus (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 10

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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