Homozygous hereditary elliptocytosis 1153399000
SNOMED CT code
| SNOMED code | 1153399000 |
|---|---|
| name | Homozygous hereditary elliptocytosis |
| status | active |
| date introduced | 2021-07-31 |
| fully specified name(s) | Homozygous hereditary elliptocytosis (disorder) |
| synonyms | Homozygous hereditary elliptocytosis |
| attributes - group3 | |
| Interprets | Measurement of total hemoglobin concentration 441689006 |
| Has interpretation | Below reference range 281300000 |
| attributes - group1 | |
| Associated morphology | Elliptocyte 45028007 |
| Finding site | Erythrocyte 41898006 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| attributes - group4 | |
| Interprets | Hemolysis 404227002 |
| Has interpretation | Present 52101004 |
| attributes - group2 | |
| Interprets | Red blood cell count 14089001 |
| Has interpretation | Below reference range 281300000 |
| parents | Hereditary elliptocytosis 191169008 |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Hereditary elliptocytosis 191169008 Homozygous hereditary elliptocytosis 1153399000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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