Autosomal recessive hereditary disorder	Deficiency of N-acetylgalactosamine-4-sulfatase	Developmental hereditary disorder	Mucopolysaccharidosis	Short stature disorder
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Maroteaux-Lamy syndrome (disorder)
	Maroteaux-Lamy syndrome
	Mucopolysaccharidosis, MPS-VI Mucopolysaccharidosis chondroitin sulfate B ARSB deficiency ARSB - Arylsulfatase B deficiency Arylsulfatase B deficiency Mucopolysaccharidosis type VI Polydystrophic dwarfism N-acetylgalactosamine-4-sulfatase deficiency MPS VI - Mucopolysaccharidosis VI Maroteaux-Lamy disease
	mucopolysacharidose type 6
	syndroom van Maroteaux-Lamy N-acetylgalactosamine-4-sulfatasedeficiëntie

Id	69463008
Status	Primitive

Finding site	Structure of nervous system
Occurrence	Congenital
Pathological process	Pathological developmental process

Interprets

Height / growth measure

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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Maroteaux-Lamy syndrome, intermediate form

Maroteaux-Lamy syndrome, mild form

Maroteaux-Lamy syndrome, severe form