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373420004: Upshaw-Schulman syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
1198718017 Upshaw-Schulman syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
1211899017 Upshaw-Schulman syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
1216561016 Familial thrombotic thrombocytopenic purpura / haemolytic uraemic syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
1218052015 Familial thrombotic thrombocytopenic purpura / hemolytic uremic syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
1229241011 Familial TTP/HUS en Synonym Active Only initial character case insensitive SNOMED CT core module
5150505018 Congenital ADAMTS-13 deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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