congenitaal defect in glycosylering type II
congenitale immunodeficiëntie
primaire immunodeficiëntie
X-gebonden hereditaire recessieve aandoening
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ATPase H+ transporting accessory protein 1 congenital disorder of glycosylation (disorder)
ATPase H+ transporting accessory protein 1 congenital disorder of glycosylation
CDG (congenital disorder of glycosylation) hepatopathy, hypogammaglobulinemia, metabolic cutis laxa syndrome
Carbohydrate deficient glycoprotein syndrome due to ATP6AP1
Congenital disorder of glycosylation type 2s
ATP6AP1-CDG - ATPase H+ transporting accessory protein 1 congenital disorder of glycosylation
Id1402318005
StatusPrimitive
Occurrencecongenitaal
Pathological processafwijkend immuunproces
SNOMED CT to ICD-10 extended map
TargetE77.8
RuleTRUE
AdviceALWAYS E77.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified