Autosomal recessive hereditary disorder	Carbohydrate-deficient glycoprotein syndrome	Developmental hereditary disorder	Global developmental delay	Intellectual disability
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Early-onset epilepsy, intellectual disability, brain anomalies syndrome (disorder)
	Early-onset epilepsy, intellectual disability, brain anomalies syndrome
	Congenital disorder of glycosylation due to phosphatidylinositol glycan anchor biosynthesis class G deficiency PIGG-CDG - congenital disorder of glycosylation due to PIGG deficiency Congenital disorder of glycosylation due to PIGG (phosphatidylinositol glycan anchor biosynthesis class G) deficiency
	A rare congenital disorder of glycosylation with characteristics of early onset of hypotonia, severe global developmental delay, intellectual disability, and seizures. Ataxia, mild facial dysmorphism and autistic behavior have also been reported. Brain MRI findings are variable and include cerebral atrophy, cerebellar hypoplasia/atrophy and thin corpus callosum.
	syndroom van vroeg optredende epilepsie, verstandelijke beperking en afwijking van hersenen
	syndroom van vroeg optredende epilepsie, verstandelijke handicap en hersenafwijking syndroom van vroeg optredende epilepsie, mentale retardatie en hersenafwijking

Id	1172627007
Status	Primitive

Occurrence	Congenital
Pathological process	Pathological developmental process

ICD-10 complex map reference set

Target	E77.8
Rule	TRUE
Advice	ALWAYS E77.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified