Upshaw-Schulman syndrome 373420004
SNOMED CT code
| SNOMED code | 373420004 |
|---|---|
| name | Upshaw-Schulman syndrome |
| status | active |
| date introduced | 2002-07-31 |
| fully specified name(s) | Upshaw-Schulman syndrome (disorder) |
| synonyms |
|
| attributes - group8 | |
| Finding site | Erythrocyte 41898006 |
| attributes - group7 | |
| Associated morphology | Schistocyte 70310009 |
| attributes - group2 | |
| Interprets | Hemostatic function 74848003 |
| Has interpretation | Abnormal 263654008 |
| attributes - group3 | |
| Interprets | Red blood cell count 14089001 |
| Has interpretation | Below reference range 281300000 |
| attributes - group4 | |
| Interprets | Measurement of total hemoglobin concentration 441689006 |
| Has interpretation | Below reference range 281300000 |
| attributes - group5 | |
| Interprets | Platelet count 61928009 |
| Has interpretation | Below reference range 281300000 |
| attributes - group6 | |
| Interprets | Hemolysis 404227002 |
| Has interpretation | Present 52101004 |
| attributes - group1 | |
| Finding site | Skin structure 39937001 |
| Associated morphology | Purpura 12393003 |
| attributes - group9 | |
| Finding site | Structure of arteriole 28225005 |
| Associated morphology | Microthrombus 446569001 |
| attributes - group10 | |
| Finding site | Structure of capillary blood vessel 20982000 |
| Associated morphology | Microthrombus 446569001 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Functional finding 118228005 Disorder of hemostatic system 362970003 Platelet disorder 22716005 Inherited platelet disorder 234469001 Upshaw-Schulman syndrome 373420004 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Cardiovascular system hereditary disorder 363005004 Upshaw-Schulman syndrome 373420004 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Upshaw-Schulman syndrome 373420004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Red blood cell disorder 38292009 Hereditary red blood cell disorder 414394009 Upshaw-Schulman syndrome 373420004 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Disorder of hemostatic system 362970003 Purpuric disorder 387778001 Thrombocytopenic purpura 302873008 Thrombotic thrombocytopenic purpura 78129009 Upshaw-Schulman syndrome 373420004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Upshaw-Schulman syndrome 373420004 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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