Autosomal recessive hereditary disorder	Disorder of glycoprotein metabolism	Dysostosis multiplex group	Lipid storage disease	Mucolipidosis
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I-cell disease (disorder)
	I-cell disease
	I-cell - Inclusion cell disease N-acetylglucosamine-1-phosphotransferase deficiency Mucolipidosis II Mucolipidosis type II
	mucolipidose 2
	'I-cell'-ziekte mucolipidosis type 2

Id	70199000
Status	Primitive

Associated morphology	Dysplasia
Finding site	Bone structure
Occurrence	Congenital
Pathological process	Pathological developmental process

PALGA thesaurus simple reference set for pathology

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	E77.0
Rule	TRUE
Advice	ALWAYS E77.0
Correlation	SNOMED CT source code to target map code correlation not specified

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Pseudo-Hurler polydystrophy