Congenital disorder of glycosylation type 1y 733115009
SNOMED CT code
| SNOMED code | 733115009 |
|---|---|
| name | Congenital disorder of glycosylation type 1y |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Congenital disorder of glycosylation type 1y (disorder) |
| synonyms |
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| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| parents |
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| 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 Congenital disorder of glycosylation type 1y 733115009 SNOMED CT Concept 138875005 Clinical 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 Congenital disorder of glycosylation type 1y 733115009 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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