Autosomal recessive hereditary disorder	Congenital osteodystrophy	Hereditary disorder of musculoskeletal system	Metabolic bone disease	Mucopolysaccharidosis
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Morquio syndrome (disorder)
	Morquio syndrome
	Osteochondrodystrophy Chondro-osteodystrophy Morquio-Ullrich disease Morquio disease Atypical chondrodystrophy Chondrodystrophia tarda Hereditary enchondral dysostosis Familial osseous dystrophy Keratan sulfaturia Brailsford-Morquio syndrome Osteochondrodystrophia deformans Familial osteochondrodystrophy Mucopolysaccharidosis type IV Morquio-Brailsford disease Mucopolysaccharidosis, MPS-IV Morquio-Suarez syndrome
	mucopolysacharidose type 4
	syndroom van Morquio
	syndroom van Morquio
	Erfelijke stofwisselingsziekte gekenmerkt door skeletafwijkingen, oogproblemen en een grof gezicht; een van de vormen van mucopolysacharidose.

Id	378007
Status	Primitive

Associated morphology	Dystrophy
Finding site	Bone structure
Occurrence	Congenital

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	E76.2
Rule	TRUE
Advice	ALWAYS E76.2
Correlation	SNOMED CT source code to target map code correlation not specified

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Mucopolysaccharidosis, MPS-IV-A

Mucopolysaccharidosis, MPS-IV-B