autosomaal recessieve hereditaire aandoening	congenitaal defect in glycosylering type I
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congenitaal defect in glycosylering type 1g (aandoening)
	congenitaal defect in glycosylering type 1g
	ALG-12-CDG congenital disorder of glycosylation type 1g
	ALG12-congenital disorder of glycosylation
	Congenital disorder of glycosylation type Ig Congenital disorder of glycosylation type 1G

Id	711155008
Status	Primitive

Occurrence

DHD Diagnosis thesaurus reference set

SNOMED CT to Orphanet simple map

79324

SNOMED CT to ICD-10 extended map

Target	E77.8
Rule	TRUE
Advice	ALWAYS E77.8
Correlation	SNOMED CT source code to target map code correlation not specified