Familial platelet syndrome with predisposition to acute myelogenous leukemia 725034002
SNOMED CT code
SNOMED code | 725034002 |
---|---|
name | Familial platelet syndrome with predisposition to acute myelogenous leukemia |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder) |
synonyms |
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attributes - group2 | |
Interprets | Hemostatic function 74848003 |
Has interpretation | Abnormal 263654008 |
attributes - group1 | |
Finding site | Structure of hematological system 414387006 |
attributes - group3 | |
Occurrence | Congenital 255399007 |
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 Familial platelet syndrome with predisposition to acute myelogenous leukemia 725034002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Platelet storage pool defect 128099001 Dense body defect 234474009 Familial platelet syndrome with predisposition to acute myelogenous leukemia 725034002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Hereditary cancer-predisposing syndrome 699346009 Familial platelet syndrome with predisposition to acute myelogenous leukemia 725034002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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