Emberger syndrome 700057001
SNOMED CT code
SNOMED code | 700057001 |
---|---|
name | Emberger syndrome |
status | active |
date introduced | 2014-01-31 |
fully specified name(s) | Emberger syndrome (disorder) |
synonyms |
|
attributes - group2 | |
Associated morphology | Lymphatic edema 30213001 |
Finding site | Limb structure 66019005 |
Pathological process | Pathological developmental process 308490002 |
attributes - group1 | |
Finding site | Bone marrow structure 14016003 |
Associated morphology | Acute myeloid leukemia myelodysplasia related 128827005 |
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 Emberger syndrome 700057001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Primary lymphedema 1217009002 Hereditary lymphedema 254199006 Emberger syndrome 700057001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Emberger syndrome 700057001 SNOMED CT Concept 138875005 Clinical finding 404684003 Mass of body structure 300848003 Mass of lymphoreticular structure 300853008 Neoplasm of bone marrow 414824005 Myeloid leukemia 188732008 Acute myeloid leukemia, disease 91861009 Acute myeloid leukemia with myelodysplasia-related changes 445448008 Emberger syndrome 700057001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Hereditary cancer-predisposing syndrome 699346009 Emberger syndrome 700057001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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