WT limb blood syndrome 719019000
SNOMED CT code
| SNOMED code | 719019000 |
|---|---|
| name | WT limb blood syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | WT limb blood syndrome (disorder) |
| synonyms | WT limb blood syndrome |
| attributes - group4 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Aplasia 45486003 |
| Finding site | Bone marrow structure 14016003 |
| attributes - group8 | |
| Pathological process | Abnormal immune process 769247005 |
| attributes - group7 | |
| Interprets | Hemostatic function 74848003 |
| Has interpretation | Abnormal 263654008 |
| attributes - group2 | |
| Has interpretation | Below reference range 281300000 |
| Interprets | White blood cell count 767002 |
| attributes - group5 | |
| Has interpretation | Below reference range 281300000 |
| Interprets | Red blood cell count 14089001 |
| attributes - group3 | |
| Has interpretation | Below reference range 281300000 |
| Interprets | Platelet count 61928009 |
| attributes - group1 | |
| Has interpretation | Below reference range 281300000 |
| Interprets | Measurement of total hemoglobin concentration 441689006 |
| attributes - group6 | |
| Due to | Decreased erythrocyte production 18469004 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 WT limb blood syndrome 719019000 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Disorder of hemostatic system 362970003 Platelet disorder 22716005 Inherited platelet disorder 234469001 WT limb blood syndrome 719019000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital anemia 63565007 Constitutional aplastic anemia 28975000 WT limb blood syndrome 719019000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 WT limb blood syndrome 719019000 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of blood, lymphatics and immune system 299691001 Disorder of cellular component of blood 414022008 White blood cell disorder 54097007 Hereditary white blood cell disorder 414395005 WT limb blood syndrome 719019000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Multiple malformation syndrome with limb defect as major feature 41443008 WT limb blood syndrome 719019000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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