ALG12-congenital disorder of glycosylation 711155008
SNOMED CT code
| SNOMED code | 711155008 |
|---|---|
| name | ALG12-congenital disorder of glycosylation |
| status | active |
| date introduced | 2015-07-31 |
| fully specified name(s) | ALG12-congenital disorder of glycosylation (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Disorder of glycoprotein metabolism 238045003 Carbohydrate-deficient glycoprotein syndrome 238049009 Carbohydrate-deficient glycoprotein syndrome type I 277893002 ALG12-congenital disorder of glycosylation 711155008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 ALG12-congenital disorder of glycosylation 711155008 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com