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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)
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Gangliosidoses
Wolman disease
Wolman disease
Fabry disease
Gaucher's disease
Krabbe disease
Niemann-Pick disease, type C
Niemann–Pick disease
Sandhoff disease
Schindler disease
Tay-Sachs disease
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Lysosomal storage diseases
(39)
Cholesteryl ester storage disease
Galactosam- ine-6-sulfatase deficiency
Metachromatic leukodystrophy
Mucopolysa- ccharidosis, type II
Alpha-mannosidosis
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidoses
Gaucher's disease
Glycogen storage disease type II
Glycoproteinosis
Hurler syndrome
I-cell disease
Krabbe disease
Lipid storage disorder
Lysosomal storage disease
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
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...
Autosomal recessive disorders
(12)
Tay-sachs disease, ab variant
Cerebrotendineous xanthomatosis
Pyrroline carboxylate dehydrogenase deficiency
McArdle syndrome
MTP deficiency
MTP deficiency
Pancreatic Insufficiency And Bone Marrow Dysfunction
Pyroglutamic aciduria
Farber disease
Gangliosidoses
Wolman disease
Metachromatic leukodystrophy
Galactosam- ine-6-sulfatase deficiency
more...
Genodermatoses
Neurofibromatosis type 3
CST syndrome
Deletion 4p
Steroid sulfatase deficiency
Distal arthrogryposis type 2A
Ichthyosis
Ichthyosis hystrix
Rare diseases
(13)
Perheentupa syndrome
Megalencephaly with hyaline inclusion
Tay-sachs disease, ab variant
GM1 gangliosidoses
GM2 gangliosidoses
GM2 gangliosidoses
Farber disease
Cholesteryl ester storage disease
Gangliosidoses
Wolman disease
Metachromatic leukodystrophy
Galactosam- ine-6-sulfatase deficiency
Pyroglutamic aciduria
Ichthyosis hystrix
more...
Genetic disorders
(25)
Niemann-Pick disease, SMPD1-associated
Jansky-bielschowsky disease
Muscular dystrophy - Duchenne type
Myopathy, Mitochondr- ial-Encephalopathy-Lactic Acidosis-Stroke
Metatropic dysplasia type II
Metatropic dysplasia type II
Tay-sachs disease, ab variant
Cerebrotendineous xanthomatosis
GM1 gangliosidoses
GM2 gangliosidoses
Farber disease
Cholesteryl ester storage disease
Gangliosidoses
Perheentupa syndrome
Wolman disease
Mucopolysa- ccharidosis, type II
Megalencephaly with hyaline inclusion
Deletion 4p
Pyrroline carboxylate dehydrogenase deficiency
McArdle syndrome
MTP deficiency
Metachromatic leukodystrophy
Pancreatic Insufficiency And Bone Marrow Dysfunction
Galactosam- ine-6-sulfatase deficiency
Pyroglutamic aciduria
Ichthyosis hystrix
more...
Diseases and disorders
(87)
Sea-blue histiocyte syndrome
Sphingolipidoses
Intestinal pseudoobstruction chronic idiopathic
N-acetyl-g- lucosamine-6-sulfate sulfatase deficiency
Narrow oral fissure short stature cone shaped epiphyses
Narrow oral fissure short stature cone shaped epiphyses
Nephropathy familial with hyperuricemia
Nephrosis deafness urinary tract digital malformation
Nephrotic syndrome ocular anomalies
Neuraminidase beta-galactosidase deficiency
Neuronal interstitial dysplasia
Neuropathy motor sensory type 2 deafness mental retardation
Neuropathy sensory spastic paraplegia
Neutropenia monocytopenia deafness
Nevus of ota retinitis pigmentosa
Night blindness skeletal anomalies unusual facies
Noble bass sherman syndrome
Non-lissencephalic cortical dysplasia
Noninsulin- -dependent diabetes mellitus with deafness
Nose polyposis familial
Chromosome 9 partial trisomy 9p
Congenital generalized phlebectasia
Nakamura osame syndrome
Nanism due to growth hormone combined deficiency
Neuhauser eichner opitz syndrome
Novak syndrome
Chromosome 4 monosomy distal 4q
Chromosome 9 partial monosomy 9p
Chromosome 7 partial monosomy 7p
Megalocornea mental retardation syndrome
Calcium pyrophosphate arthropathy
Myopathy desmin storage
Chromosome 9 tetrasomy 9p
Neuroaxonal dystrophy renal tubular acidosis
Chromosome 3 trisomy 3q2
Chromosome 4 partial trisomy distal 4q
Chronic spasmodic dysphonia
Chromosome 4 monosomy 4q
Nephronophthisis familial adult spastic quadriparesis
Nephropathy deafness hyperparathyroidism
Neutropenia intermittent
Ilyina amoashy grygory syndrome
Imperforate oropharynx costo vetebral anomalies
Infantile striato thalamic degeneration
Intestinal malrotation facial anomalies familial type
Isthmian coarctation
Primary renal glycosuria
Myoclonic progressive familial epilepsy
Chromosome 8 monosomy 8p2
Muscular dystrophies, limb-girdle
Dentin dysplasia coronal
Maxillonasal dysplasia binder type
major aphthous ulcer
Alpha b lysosomal mannosidosis
Delleman oorthuys syndrome
Donath-Landsteiner syndrome
Chromosomal triplication
Polyglucosan body disease adult
Congenital craniosynostosis maternal hyperthyroiditis
Congenital heart disease ptosis hypodontia craniostosis
Macular degeneration polymorphic
Poliodystrophia cerebri
Massive myoclonia
Paracoccidioidal granuloma
Cerebrotendineous xanthomatosis
GM1 gangliosidoses
Jansky-bielschowsky disease
GM2 gangliosidoses
Farber disease
Cholesteryl ester storage disease
Gangliosidoses
Wolman disease
Muscular dystrophy - Duchenne type
Neurofibromatosis type 3
Mucopolysa- ccharidosis, type II
Megalencephaly with hyaline inclusion
CST syndrome
Steroid sulfatase deficiency
Pyrroline carboxylate dehydrogenase deficiency
Myopathy, Mitochondr- ial-Encephalopathy-Lactic Acidosis-Stroke
MTP deficiency
Metatropic dysplasia type II
Metachromatic leukodystrophy
Distal arthrogryposis type 2A
Pancreatic Insufficiency And Bone Marrow Dysfunction
Galactosam- ine-6-sulfatase deficiency
Ichthyosis
Lysosomal storage diseases
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...
See also
(12)
Iduronate sulfatase
Proteins
Midface trauma
SUMF1
Sulfatases
Sulfatases
Pfeiffer-W- eber-Christian syndrome
CFTDM
Linear epidermal nevus
Anemia, macrocytic
Maxillonasal dysplasia
Sphingolipids
Chemical substances
more...
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