congenitaal defect in glycosylering type 1A (aandoening)
	congenitaal defect in glycosylering type 1A
	fosfomannomutase-2-deficiëntie congenital disorder of glycosylation type 1a
	Congenital disorder of glycosylation type Ia

Id	459063003
Status	Primitive

Occurrence

Due to

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	E77.8
Term	Overige gespecificeerde stoornissen van glycoproteïnemetabolisme

SNOMED CT to Orphanet simple map

79318

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