Brunner syndrome 718210003
SNOMED CT code
| SNOMED code | 718210003 |
|---|---|
| name | Brunner syndrome |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | Deficiency of monoamine oxidase A (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Finding site | Nervous system structure 25087005 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked recessive hereditary disease 1162976004 Brunner syndrome 718210003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Inherited metabolic disorder of nervous system 128190004 Brunner syndrome 718210003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Enzymopathy 78548001 Specific enzyme deficiency 129456006 Deficiency of tyraminase 361094004 Brunner syndrome 718210003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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