Search on: MUCOPOLYSACCHARIDOSIS VI 
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Descriptor English:   Mucopolysaccharidosis VI 
Descriptor Spanish:   Mucopolisacaridosis VI 
Descriptor Portuguese:   Mucopolissacaridose VI 
Synonyms English:   ARSB Deficiencies
ARSB Deficiency
Arylsulfatase B Deficiencies
Arylsulfatase B Deficiency
Deficiencies, ARSB
Deficiencies, Arylsulfatase B
Deficiencies, N-Acetylgalactosamine-4-Sulfatase
Deficiency, ARSB
Deficiency, Arylsulfatase B
Deficiency, N-Acetylgalactosamine-4-Sulfatase
Dwarfism, Polydystrophic
Maroteaux Lamy Syndrome
Maroteaux-Lamy Syndrome
Mucopolysaccharidosis 6
Mucopolysaccharidosis Type 6
Mucopolysaccharidosis Type VI
N-Acetylgalactosamine-4-Sulfatase Deficiencies
N-Acetylgalactosamine-4-Sulfatase Deficiency
Polydystrophic Dwarfism
Syndrome, Maroteaux-Lamy
Type 6, Mucopolysaccharidosis
Type VI, Mucopolysaccharidosis  
Tree Number:   C16.320.565.202.715.670
C16.320.565.595.600.670
C17.300.550.575.670
C18.452.648.202.715.670
C18.452.648.595.600.670
Definition English:   Mucopolysaccharidosis with excessive CHONDROITIN SULFATE B in urine, characterized by dwarfism and deafness. It is caused by a deficiency of N-ACETYLGALACTOSAMINE-4-SULFATASE (arylsulfatase B). 
History Note English:   92; was MUCOPOLYSACCHARIDOSIS 6 1991; was see under MUCOPOLYSACCHARIDOSIS 1975-90 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DG diagnostic imaging DH diet therapy
DT drug therapy EC economics
EM embryology EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RT radiotherapy
RH rehabilitation SU surgery
TH therapy UR urine
VE veterinary VI virology
Record Number:   30391 
Unique Identifier:   D009087 

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