Mucopolysaccharidosis III
Mucopolysaccharidosis characterized by heparitin sulfate in the urine, progressive mental retardation, mild dwarfism, and other skeletal disorders. There are four clinically indistinguishable but biochemically distinct forms, each due to a deficiency of a different enzyme.
推出的年份: 1992
树号: C16.320.565.202.715.650, C16.320.565.595.600.650, C17.300.550.575.650, C18.452.648.202.715.650, C18.452.648.595.600.650
MeSH 单一 ID: D009084
进入的组:
Mucopolysaccharidosis IIIs
Sanfilippo Syndrome
Sanfilippo Syndromes
Syndrome, Sanfilippo
Syndromes, Sanfilippo
Mucopolysaccharidosis 3
San Filippo's Syndrome
San Filippo Syndrome
San Filippos Syndrome
Syndrome, San Filippo's
Polydystrophic Oligophrenia
Oligophrenia, Polydystrophic
Oligophrenias, Polydystrophic
Polydystrophic Oligophrenias
Sanfilippo's Syndrome
Sanfilippos Syndrome
Syndrome, Sanfilippo's
MPS III D
Mucopolysaccharidosis Type 3 D
Mucopolysaccharidosis Type IIID
Mucopolysaccharidosis Type IIIDs
Sanfilippo Syndrome D
N-Acetylglucosamine-6-Sulfatase Deficiency
Deficiencies, N-Acetylglucosamine-6-Sulfatase
Deficiency, N-Acetylglucosamine-6-Sulfatase
N Acetylglucosamine 6 Sulfatase Deficiency
N-Acetylglucosamine-6-Sulfatase Deficiencies
MPS IIID
MPS IIIDs
MPS 3 D
N-Acetylglucosamine-6-Sulfate Sulfatase Deficiency
Deficiencies, N-Acetylglucosamine-6-Sulfate Sulfatase
Deficiency, N-Acetylglucosamine-6-Sulfate Sulfatase
N Acetylglucosamine 6 Sulfate Sulfatase Deficiency
N-Acetylglucosamine-6-Sulfate Sulfatase Deficiencies
Sulfatase Deficiencies, N-Acetylglucosamine-6-Sulfate
Sulfatase Deficiency, N-Acetylglucosamine-6-Sulfate
MPS III C
Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase Deficiency
Acetyl CoA:alpha Glucosaminide N Acetyltransferase Deficiency
Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase Deficiencies
Deficiencies, Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase
Deficiency, Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase
N-Acetyltransferase Deficiencies, Acetyl-CoA:alpha-Glucosaminide
N-Acetyltransferase Deficiency, Acetyl-CoA:alpha-Glucosaminide
Mucopolysaccharidosis Type IIIC
Mucopolysaccharidosis Type IIICs
MPS 3 C
MPS3C
MPS IIIC
Mucopolysaccharidosis Type 3 C
Sanfilippo Syndrome C
MPS III A
MPS 3 A
Mucopolysaccharidosis Type 3 A
Mucopolysaccharidosis Type IIIA
Mucopolysaccharidosis Type IIIAs
Sanfilippo Syndrome A
Mucopolysaccharidosis Type 3 A Sanfilippo Syndrome
Sulfamidase Deficiency
Deficiencies, Sulfamidase
Deficiency, Sulfamidase
Sulfamidase Deficiencies
MPS IIIA
MPS3A
Heparan Sulfate Sulfatase Deficiency
MPS III B
Sanfilippo Syndrome B
MPS3B
Mucopolysaccharidosis Type IIIB
Mucopolysaccharidosis Type IIIBs
NAGLU Deficiency
Deficiencies, NAGLU
Deficiency, NAGLU
NAGLU Deficiencies
N-Acetyl-alpha-D-Glucosaminidase Deficiency
Deficiencies, N-Acetyl-alpha-D-Glucosaminidase
Deficiency, N-Acetyl-alpha-D-Glucosaminidase
N Acetyl alpha D Glucosaminidase Deficiency
N-Acetyl-alpha-D-Glucosaminidase Deficiencies
MPS IIIB
Mucopolysaccharidosis Type 3 B
MPS 3 B
早前的内容:
Carbohydrate Metabolism, Inborn Errors (1966-1976)
Mental Retardation (1966-1976)
Mucopolysaccharides/metabolism (1966-1974)
Mucopolysaccharidosis (1974)
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