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Multiple Sulfatase Deficiency
Multiple sulfatase deficiency
Overview
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Related in the Kosmos
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Lipid storage disorders
(13)
Fabry's disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Gangliosidoses
Gangliosidoses
Krabbe disease
Sandhoff disease
Wolman disease
Gaucher's disease
Niemann-Pick disease, type C
Niemann–Pick disease
Schindler disease
Tay-Sachs disease
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Autosomal recessive disorders
(17)
Tay-sachs disease, ab variant
Cerebrotendineous xanthomatosis
Metachromatic leukodystrophy
McArdle syndrome
Mucopolysa- ccharidosis
Mucopolysa- ccharidosis
Mucopolysa- ccharidosis, type I
Congenital ichthyosiform erythroderma
Batten disease
Mucolipidosis
Carnitine deficiency
Sanfilippo syndrome
Neuronal ceroid lipofuscinosis
Farber disease
Gangliosidoses
Wolman disease
Sandhoff disease
Krabbe disease
more...
Genodermatoses
(8)
Benign familial pemphigus
Erythrokeratodermia variabilis
X-linked ichthyosis
Peeling skin syndrome
Sjogren-larsson syndrome
Sjogren-larsson syndrome
Refsum disease
Chondrodysplasia punctata
Congenital ichthyosiform erythroderma
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Rare diseases
(14)
Cholesteryl ester storage disease
Tay-sachs disease, ab variant
GM1 gangliosidoses
GM2 gangliosidoses
Farber disease
Farber disease
Gangliosidoses
Metachromatic leukodystrophy
Wolman disease
Fabry's disease
Sandhoff disease
Congenital ichthyosiform erythroderma
Krabbe disease
Sanfilippo syndrome
Neuronal ceroid lipofuscinosis
more...
Lysosomal storage diseases
(39)
Lysosomal storage disorders
Mucopolysa- ccharidosis, type II
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cystinosis
Fabry's disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidoses
Gaucher's disease
Glycogen storage disease type II
Glycoproteinosis
I-cell disease
Krabbe disease
Lipid storage disorder
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Mucopolysa- ccharidosis, type I
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
more...
Genetic disorders
(29)
Niemann-Pick disease, SMPD1-associated
Jansky-bielschowsky disease
Fukuyama type muscular dystrophy
Muscular dystrophy - Duchenne type
Partial monosomy
Partial monosomy
Hereditary disorder
X-linked adrenoleuk- odystrophy
Porphyria cutanea tarda
Tay-sachs disease, ab variant
Cerebrotendineous xanthomatosis
GM1 gangliosidoses
GM2 gangliosidoses
Cholesteryl ester storage disease
Farber disease
Gangliosidoses
Metachromatic leukodystrophy
Wolman disease
McArdle syndrome
Mucopolysa- ccharidosis
Fabry's disease
Mucopolysa- ccharidosis, type II
Sandhoff disease
Mucopolysa- ccharidosis, type I
Congenital ichthyosiform erythroderma
Batten disease
Mucolipidosis
Krabbe disease
Carnitine deficiency
Sanfilippo syndrome
more...
Diseases and disorders
(72)
Sea-blue histiocyte syndrome
Nakamura osame syndrome
Nanism due to growth hormone combined deficiency
Narrow oral fissure short stature cone shaped epiphyses
Nephronophthisis familial adult spastic quadriparesis
Nephronophthisis familial adult spastic quadriparesis
Nephropathy deafness hyperparathyroidism
Nephropathy familial with hyperuricemia
Nephrosis deafness urinary tract digital malformation
Nephrotic syndrome ocular anomalies
Neuhauser eichner opitz syndrome
Neuraminidase beta-galactosidase deficiency
Neuroaxonal dystrophy renal tubular acidosis
Neuroma biliary tract
Neuronal interstitial dysplasia
Neuropathy motor sensory type 2 deafness mental retardation
Neuropathy sensory spastic paraplegia
Neutropenia intermittent
Neutropenia monocytopenia deafness
Night blindness skeletal anomalies unusual facies
Noble bass sherman syndrome
Non-lissencephalic cortical dysplasia
Noninsulin- -dependent diabetes mellitus with deafness
Nose polyposis familial
Novak syndrome
Sulfatidosis
Morvan disease
N-acetyl-g- lucosamine-6-sulfate sulfatase deficiency
Metatropic dwarfism
Netherton syndrome ichthyosis
Mesangiocapillary glomerulonephritis
Ichthyosis hystrix curth macklin type
Marinesco sjogren syndrome
Sphingolipidoses
Megarectum
Mucous retention cyst
Maroteaux-Lamy syndrome
Myopathy
Myotubular myopathy
Malignant melanoma
Metrorrhagia
Aplasia
Cerebrotendineous xanthomatosis
GM1 gangliosidoses
Jansky-bielschowsky disease
GM2 gangliosidoses
Cholesteryl ester storage disease
Farber disease
Fukuyama type muscular dystrophy
Gangliosidoses
Metachromatic leukodystrophy
Muscular dystrophy - Duchenne type
Wolman disease
Benign familial pemphigus
Mucopolysa- ccharidosis
Fabry's disease
Mucopolysa- ccharidosis, type II
X-linked ichthyosis
Sandhoff disease
Mucopolysa- ccharidosis, type I
Peeling skin syndrome
Lysosomal storage diseases
Sjogren-larsson syndrome
Batten disease
Mucolipidosis
Refsum disease
Chondrodysplasia punctata
Krabbe disease
Partial monosomy
Carnitine deficiency
Sanfilippo syndrome
Neuronal ceroid lipofuscinosis
Porphyria cutanea tarda
more...
Metabolic disorders
(60)
Activated protein C resistance
Adenosine deaminase deficiency
Albinism
Alcohol flush reaction
Antithrombin III deficiency
Antithrombin III deficiency
Baker IDI Heart and Diabetes Institute
Blue diaper syndrome
Childhood obesity
Congenital disorder of glycosylation
Congenital hyperinsulinism
Crigler-Najjar syndrome
Diagnostic fast
Disaccharidase
Disorders of calcium metabolism
Ectopic calcification
Farber disease
Fructose malabsorption
GM1 gangliosidoses
GM2 gangliosidoses
Galactosemia
Galactosemic cataract
Gangliosidoses
Gaucher's disease
Glycogen storage disease type 0
Hereditary fructose intolerance
Homocystinuria
Hyperglycemia
Hyperinsulinemic hypoglycemia
Hyperinsulinism
Hypoglycemia
Inborn errors of metabolism
Ketotic hypoglycemia
Krabbe disease
Lactose intolerance
Lipid storage disorders
List of causes of hypoglycemia
Metab-L
Methemoglobinemia
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Obesity
Obesogen
Pickardt syndrome
Pycnodysostosis
Refeeding syndrome
Richner Hanhart syndrome
Rotor syndrome
Salicylate sensitivity
Schindler disease
Selfish Brain Theory
Sitosterolemia
Stress hyperglycemia
Sucrose intolerance
Tay-Sachs disease
Triosephosphate isomerase deficiency
Urbach–Wiethe disease
Urea cycle disorder
Winchester syndrome
Wolman disease
more...
Leukodystrophies
Alexander disease
Canavan disease
Krabbe disease
Metachromatic leukodystrophy
Pelizaeus-- Merzbacher disease
X-linked adrenoleuk- odystrophy
Zellweger syndrome
See also
(20)
Midface trauma
Iduronate sulfatase
Proteins
Sulfatases
SUMF1
SUMF1
Anemia, macrocytic
Muscle glycogen phosphorylase
Glycolipid
Cerebrosid- e-sulfatase
Autosomal recessive
Sphingolipids
Mullerian duct
Chemical substances
Sulfatide
Ceramide
Comprehensive metabolic panel
Coarse facial features
Cornification
Arylsulfatase B
Myelin
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