Pelger-Huët anomaly 85559002
SNOMED CT code
| SNOMED code | 85559002 |
|---|---|
| name | Pelger-Huët anomaly |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Pelger-Huët anomaly (disorder) |
| synonyms |
|
| attributes - group3 | |
| Pathological process | Abnormal immune process 769247005 |
| attributes - group1 | |
| Interprets | White blood cell test 252305002 |
| attributes - group2 | |
| Interprets | Genetic test 405824009 |
| parents | |
| children | Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome 1237618009 |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Finding of blood, lymphatics and immune system 299691001 Immune system finding 106182000 White blood cell finding 250271003 Neutrophil abnormality 250274006 Pelger-Huët cell 15111002 Pelger-Huët anomaly 85559002 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 Non-malignant white cell disorder 234414004 Pelger-Huët anomaly 85559002 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 Qualitative abnormality of granulocyte 319171004 Pelger-Huët anomaly 85559002 SNOMED CT Concept 138875005 Clinical finding 404684003 Procedure related finding 127325009 Evaluation finding 441742003 Genetic finding 106221001 Genetic anomaly of leukocyte 47986005 Pelger-Huët anomaly 85559002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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