Hereditary elliptocytosis due to glycophorin C deficiency 15121005
SNOMED CT code
SNOMED code | 15121005 |
---|---|
name | Hereditary elliptocytosis due to glycophorin C deficiency |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Hereditary elliptocytosis due to glycophorin C deficiency (disorder) |
synonyms | Hereditary elliptocytosis due to glycophorin C deficiency |
attributes - group3 | |
Interprets | Hemolysis 404227002 |
Has interpretation | Present 52101004 |
attributes - group4 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Erythrocyte 41898006 |
Associated morphology | Elliptocyte 45028007 |
attributes - group1 | |
Has interpretation | Below reference range 281300000 |
Interprets | Measurement of total hemoglobin concentration 441689006 |
attributes - group2 | |
Has interpretation | Below reference range 281300000 |
Interprets | Red blood cell count 14089001 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Hereditary elliptocytosis 191169008 Hereditary elliptocytosis due to glycophorin C deficiency 15121005 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of blood, lymphatics and immune system 299691001 Disorder of cellular component of blood 414022008 Anemia 271737000 Anemia due to intrinsic red cell abnormality 323666000 Hereditary elliptocytosis due to glycophorin C deficiency 15121005 |
ancestors | sorted most to least specific
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cpt crosswalks |
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