Carbohydrate deficient glycoprotein syndrome type II due to MAN1B1 deficiency 733450008
SNOMED CT code
SNOMED code | 733450008 |
---|---|
name | Carbohydrate deficient glycoprotein syndrome type II due to MAN1B1 deficiency |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Carbohydrate deficient glycoprotein syndrome type 2 due to deficiency of mannosidase alpha class 1B member 1 (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 II 277894008 Carbohydrate deficient glycoprotein syndrome type II due to MAN1B1 deficiency 733450008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Carbohydrate deficient glycoprotein syndrome type II due to MAN1B1 deficiency 733450008 |
ancestors | sorted most to least specific
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cpt crosswalks |
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