congenitaal defect in glycosylering
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congenitaal defect in glycosylering type I (aandoening)
congenitaal defect in glycosylering type I
CDG-syndroom type I
syndroom van Jaeken
Carbohydrate-deficient glycoprotein syndrome type I
CDG - Carbohydrate-deficient glycoprotein syndrome type I
Id277893002
StatusPrimitive
Occurrencecongenitaal
SNOMED CT to ICD-10 extended map
TargetE77.8
RuleTRUE
AdviceALWAYS E77.8
CorrelationSNOMED CT source code to target map code correlation not specified
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'asparagine-linked' congenitaal defect in glycosylering type 1D
'asparagine-linked' congenitaal defect in glycosylering type 1H
'asparagine-linked' congenitaal defect in glycosylering type 1L
'asparagine-linked' congenitaal defect in glycosylering type I
congenitaal defect in glycosylering bij fosfoglucomutase 1
congenitaal defect in glycosylering door deficiëntie van mannose-6-fosfaatisomerase
congenitaal defect in glycosylering gerelateerd aan carbamoylfosfaatsynthetase 2, aspartaattranscarbamoylase en dihydro-orotase
congenitaal defect in glycosylering type 1A
congenitaal defect in glycosylering type 1C
congenitaal defect in glycosylering type 1CC
congenitaal defect in glycosylering type 1g
congenitaal defect in glycosylering type 1p
congenitaal defect in glycosylering type 1s
congenitaal defect in glycosylering type 1y
congenitaal defect in glycosylering type Ie
congenitaal defect in glycosylering type If
congenitaal defect in glycosylering type Ig
congenitaal defect in glycosylering type Ih
congenitaal defect in glycosylering type Ii
congenitaal defect in glycosylering type Ij
congenitaal defect in glycosylering type Im
congenitaal defect in glycosylering type In
congenitaal defect in glycosylering type Io
congenitaal defect in glycosylering type Iq
congenitaal defect in glycosylering type Ir
congenitaal defect in glycosylering type Iw
congenitaal defect in glycosylering type Ix
congenitaal defect van glycosylering type 1D
congenitaal defect van glycosylering type 1E
congenitale myasthenie met defect in glycolysering door mutatie in 'ALG14 UDP-N-acetylglucosaminyltransferase subunit'-gen
congenitale spierdystrofie met verstandelijke beperking en ernstige epilepsie