Selective malabsorption of cyanocobalamin 234363001
SNOMED CT code
| SNOMED code | 234363001 |
|---|---|
| name | Selective malabsorption of cyanocobalamin |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Selective malabsorption of cyanocobalamin (disorder) |
| synonyms |
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| attributes - group3 | |
| Due to | Cobalamin deficiency 190634004 |
| 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 Procedure related finding 127325009 Evaluation finding 441742003 Hematopoietic system finding 106200001 Hemoglobin finding 250220000 Hemoglobin level outside reference range 441793007 Hemoglobin below reference range 165397008 Selective malabsorption of cyanocobalamin 234363001 SNOMED CT Concept 138875005 Clinical finding 404684003 Procedure related finding 127325009 Evaluation finding 441742003 Measurement finding 118245000 Red blood cell count - finding 365625004 Red blood cell count outside reference range 165427000 Red blood cell count below reference range 165423001 Selective malabsorption of cyanocobalamin 234363001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of organic acid metabolism 116021002 Disorder of amino acid metabolism 44779003 Disorder of amino acid and organic acid metabolism 237911005 Disorder of sulfur-bearing amino acid metabolism 28882002 Selective malabsorption of cyanocobalamin 234363001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Nutritional deficiency associated condition 363246002 Megaloblastic anemia due to vitamin B>12< deficiency 49472006 Pernicious anemia 84027009 Selective malabsorption of cyanocobalamin 234363001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Nutritional disorder 2492009 Vitamin disease 7521001 Vitamin deficiency 85670002 Selective malabsorption of cyanocobalamin 234363001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Selective malabsorption of cyanocobalamin 234363001 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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