Congenital disorder of glycosylation type 1w 733111000
SNOMED CT code
SNOMED code | 733111000 |
---|---|
name | Congenital disorder of glycosylation type 1w |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Congenital disorder of glycosylation type 1w (disorder) |
synonyms |
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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 Congenital disorder of glycosylation type 1w 733111000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Congenital disorder of glycosylation type 1w 733111000 |
ancestors | sorted most to least specific
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cpt crosswalks |
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