-
Multiple sulfatase deficiency (MSD), also
known as
Austin disease, or mucosulfatidosis, is a very rare
autosomal recessive lysosomal storage disease caused...
- In biochemistry,
sulfatases EC 3.1.6.- are a
class of
enzymes of the
esterase class that
catalyze the
hydrolysis of
sulfate esters into an
alcohol and...
-
Iduronate 2-
sulfatase (EC 3.1.6.13;
systematic name L-iduronate-2-sulfate 2-sulfohydrolase) is a
sulfatase enzyme ****ociated with
Hunter syndrome. It catalyses...
-
Steroid sulfatase (STS), or steryl-
sulfatase (EC 3.1.6.2),
formerly known as
arylsulfatase C, is a
sulfatase enzyme involved in the
metabolism of steroids...
- is a skin
condition caused by the
hereditary deficiency of the
steroid sulfatase (STS)
enzyme that
affects 1 in 2000 to 1 in 6000 males. XLI manifests...
-
syndrome is
caused by a
deficiency of the
lysosomal enzyme iduronate-2-
sulfatase (I2S). The lack of this
enzyme causes heparan sulfate and
dermatan sulfate...
-
sulfatase,
nitrocatechol sulfatase, phenolsulfatase, phenylsulfatase, p-nitrophenyl
sulfatase, arylsulfohydrolase, 4-methylumbelliferyl
sulfatase, estrogen...
- MPS IV
Morquio syndrome type Gene
Missing enzyme Chromosomal region Type A
GALNS Galactosamine-6
sulfatase 16q24 Type B GLB1 Beta-galactosidase 3p22...
- N-acetylgalactosamine-6-
sulfatase is an
enzyme that, in humans, is
encoded by the
GALNS gene. This gene
encodes N-acetylgalactosamine-6-
sulfatase,
which is a lysosomal...
- Cerebroside-
sulfatase (EC 3.1.6.8,
arylsulfatase A,
cerebroside sulfate sulfatase) is an
enzyme with
systematic name cerebroside-3-sulfate 3-sulfohydrolase...
