Kosmix
One sec... we're building your guide for
Wolman Disease
Wolman disease
Overview
Main ›
Treatments ›
Genetic Information ›
From Experts ›
Patient Experiences ›
Video ›
Images ›
News & Blogs ›
Guides & Articles ›
Reference ›
Topics Related to Wolman disease
?
Lipid storage disorders
(13)
Fabry's disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Gangliosidoses
Gangliosidoses
Kanzaki disease
Multiple sulfatase deficiency
Niemann-pick diseases
Sandhoff disease
Gaucher's disease
Krabbe disease
Niemann-Pick disease, type C
Tay-Sachs disease
more...
Metabolic disorders
(58)
Adenosine deaminase deficiency
Disorders of calcium metabolism
Inborn errors of metabolism
Neuronal ceroid lipofuscinosis
Sucrose intolerance
Sucrose intolerance
Activated protein C resistance
Albinism
Alcohol flush reaction
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
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
Kanzaki disease
Ketotic hypoglycemia
Krabbe disease
Lactose intolerance
Lipid storage disorders
List of causes of hypoglycemia
Metab-L
Methemoglobinemia
Niemann-Pick disease, type C
Niemann-pick diseases
Obesity
Pickardt syndrome
Pycnodysostosis
Refeeding syndrome
Richner Hanhart syndrome
Rotor syndrome
Salicylate sensitivity
Selfish Brain Theory
Sitosterolemia
Stress hyperglycemia
Tay-Sachs disease
Triosephosphate isomerase deficiency
Urbach–Wiethe disease
Urea cycle disorder
Winchester syndrome
more...
Neurological disorders
Leukodystrophy
Batten disease
Neuronal ceroid lipofuscinosis
Lysosomal storage diseases
(39)
Alpha-mannosidosis
Arylsulfatase A deficiency
Aspartylgl- ucosaminuria
Cholesteryl ester storage disease
Hurler-Scheie Syndrome
Hurler-Scheie Syndrome
Lipidoses
Lysosomal disease
Mucolipidosis I
Mucolipidosis II
Pseudo-Hurler polydystrophy
Scheie syndrome
Sly syndrome
Batten disease
Canavan disease
Cystinosis
Fabry's disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidoses
Gaucher's disease
Glycogen storage disease type II
Glycoproteinosis
Hunter syndrome
Kanzaki disease
Krabbe disease
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann-pick diseases
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Tay-Sachs disease
more...
Inborn errors of metabolism
(106)
3 methylcrotonyl-coa carboxylase deficiency
Acatalasia
Acid lipase deficiency
Carbamoyl phosphate synthetase I deficiency
Essential fructosuria
Essential fructosuria
Fucosidosis
Galactose-- 1-phosphate uridylyltransferase galactosemia
Glutaric acidemia type 1
Glycogen storage disease type iii
Histidinemia
Lecithin cholesterol acyltransferase deficiency
N-acetylglutamate synthase deficiency
Sarcosinemia
2,4 Dienoyl-CoA reductase deficiency
2-Methylbutyryl-CoA dehydrogenase deficiency
3-hydroxy-- 3-methylglutaryl-CoA lyase deficiency
3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Adenosine deaminase deficiency
Adenylosuccinate lyase deficiency
Aldolase A deficiency
Analbuminaemia
Arakawa's syndrome II
Argininemia
Argininosuccinic aciduria
Aspartylgl- ucosaminuria
Beta-ketothiolase deficiency
Carnitine palmitoylt- ransferase I deficiency
Carnitine palmitoylt- ransferase II deficiency
Carnitine-- acylcarnitine translocase deficiency
Cholesteryl ester storage disease
Citrullinemia
Congenital disorder of glycosylation
Crigler-Najjar syndrome
D-Glyceric acidemia
DOOR syndrome
Dihydropyrimidine dehydrogenase deficiency
Disaccharidase
Fumarase deficiency
Galactosemia
Glucose-galactose malabsorption
Glutaric acidemia type 2
Glycogen storage disease
Glycogen storage disease type I
Glycogen storage disease type II
Glycogen storage disease type V
Guanidinoacetate methyltransferase deficiency
Hawkinsinuria
Hereditary fructose intolerance
Holocarboxylase synthetase deficiency
Hyperlysinemia
Hypermethioninemia
Hyperprolinemia
Hypervalinemia
Idiosyncrasy
Inborn error of lipid metabolism
Inborn error of metabolism
Isobutyryl-coenzyme A dehydrogenase deficiency
Isovaleric acidemia
Kanzaki disease
Krabbe disease
Lesch–Nyhan syndrome
Lipid storage disorders
Lipidoses
Long-chain 3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Lysinuric protein intolerance
Lysosomal disease
Lysosomal storage diseases
Malonyl-CoA decarboxylase deficiency
Maple syrup urine disease
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Menkes disease
Metab-L
Methylmalonic acidemia
Methylmalonyl-CoA mutase deficiency
Mevalonate kinase deficiency
Mitochondrial trifunctional protein deficiency
Myoadenylate deaminase deficiency
Newborn screening
Niemann-Pick disease, type C
Organic acidemia
Ornithine transcarbamylase deficiency
Ornithine translocase deficiency
Phenylketonuria
Primary carnitine deficiency
Prolidase deficiency
Propionic acidemia
Pyruvate carboxylase deficiency
Pyruvate kinase deficiency
Refsum's disease
Rotor syndrome
Short-chain acyl-coenzyme A dehydrogenase deficiency
Sly syndrome
Smith-Lemli-Opitz syndrome
Succinic semialdehyde dehydrogenase deficiency
Tangier disease
Tetrahydrobiopterin deficiency
Trimethylaminuria
Type I tyrosinemia
Type III tyrosinemia
Tyrosinemia
Tyrosinemia type II
Urea cycle disorder
Urocanic aciduria
Very long-chain acyl-coenzyme A dehydrogenase deficiency
X-linked ichthyosis
Zellweger syndrome
more...
Autosomal recessive disorders
(248)
Abetalipop- roteinemia
Bare lymphocyte syndrome
Cartilage hair hypoplasia
Cerebrotendineous xanthomatosis
Cystathioninuria
Cystathioninuria
Glanzmann thrombasthenia
Leukocyte adhesion deficiency
Lucey-Driscoll syndrome
Tay-sachs disease, ab variant
17-beta-hy- droxysteroid dehydrogenase deficiency
2-Hydroxyglutaric aciduria
3 methylcrotonyl-coa carboxylase deficiency
Abdallat Davis Farrage syndrome
Abderhalde- n-Kaufmann-Lignac syndrome
Ablepharon macrostomia syndrome
Acatalasia
Aceruloplasminemia
Acheiropodia
Acrocallosal syndrome
Acrodermatitis enteropathica
Acute fatty liver of pregnancy
Adducted thumb syndrome
Adenine phosphorib- osyltransferase deficiency
Adenosine deaminase deficiency
Adenylosuccinate lyase deficiency
Aicardi-Goutieres syndrome
Aldolase A deficiency
Alkaptonuria
Alpha-mannosidosis
Antley-Bixler syndrome
Argininemia
Argininosuccinic aciduria
Arterial tortuosity syndrome
Arylsulfatase A deficiency
Aspartylgl- ucosaminuria
Atelosteogenesis, type II
Atransferrinemia
Batten disease
Behr's syndrome
Bernard-Soulier syndrome
Beta-ketothiolase deficiency
Beta-mannosidosis
Bietti's crystalline dystrophy
Biotinidase deficiency
Bloom syndrome
Blue diaper syndrome
CAMFAK syndrome
Canavan disease
Carbamoyl phosphate synthetase I deficiency
Carnitine palmitoylt- ransferase I deficiency
Carnitine palmitoylt- ransferase II deficiency
Carnitine-- acylcarnitine translocase deficiency
Carnosinemia
Carpenter syndrome
Cenani Lenz syndactylism
Chediak–Higashi syndrome
Chondrodystrophy
Chorea acanthocytosis
Citrullinemia
Cockayne syndrome
Compound heterozygosity
Congenital adrenal hyperplasia
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Congenital hepatic fibrosis
Congenital ichthyosiform erythroderma
Congenital insensitivity to pain with anhidrosis
Craniodiaphyseal dysplasia
Cystic fibrosis
Cystinosis
Cystinuria
D-Glyceric acidemia
DOOR syndrome
Diastrophic dysplasia
Dihydropyrimidine dehydrogenase deficiency
Donohue syndrome
Dubin-Johnson syndrome
Dubowitz syndrome
EAST syndrome
EEM syndrome
Ellis-van Creveld syndrome
Essential fructosuria
Ethylmalonic encephalopathy
Familial Mediterranean fever
Familial dysautonomia
Familial isolated vitamin E deficiency
Fanconi anemia
Farber disease
Fibrochondrogenesis
Finnish heritage disease
Fountain syndrome
Friedreich's ataxia
Fucosidosis
Fumarase deficiency
Galactokinase deficiency
Galactose epimerase deficiency
Galactose-- 1-phosphate uridylyltransferase galactosemia
Galloway Mowat syndrome
Gangliosidoses
Gastroschisis
Gaucher's disease
Gerodermia osteodysplastica
Giant axonal neuropathy
Gitelman syndrome
Glucose-galactose malabsorption
Glutaric acidemia type 1
Glutaric acidemia type 2
Glutathione synthetase deficiency
Glycogen storage disease type I
Glycogen storage disease type II
Glycogen storage disease type V
Glycogen storage disease type iii
Griscelli syndrome
Guanidinoacetate methyltransferase deficiency
Gunther disease
Hartnup disease
Hemophagocytic lymphohistiocytosis
Hereditary pyropoikilocytosis
Hermansky–Pudlak syndrome
Histidinemia
Holocarboxylase synthetase deficiency
Homocystinuria
Hurler-Scheie Syndrome
Hyperlysinemia
Hypermethioninemia
Hyperprolinemia
Hypertryptophanemia
Hypervalinemia
ICF syndrome
Ichthyosis lamellaris
Iminoglycinuria
Impossible syndrome
Infantile free sialic acid storage disease
Infantile neuroaxonal dystrophy
Isobutyryl-coenzyme A dehydrogenase deficiency
Isovaleric acidemia
Jervell and Lange-Nielsen syndrome
Johanson-Blizzard syndrome
Juvenile Primary Lateral Sclerosis
Kaufman oculocerebrofacial syndrome
Keutel syndrome
Kindler syndrome
Krabbe disease
Lafora disease
Laron syndrome
Lecithin cholesterol acyltransferase deficiency
Lipidoses
Lipoid congenital adrenal hyperplasia
Long-chain 3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Lysinuric protein intolerance
Malonyl-CoA decarboxylase deficiency
Maple syrup urine disease
Meckel syndrome
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Meleda disease
Methemoglobinemia
Methylmalonic acidemia
Mevalonate kinase deficiency
Micro syndrome
Microvillous inclusion disease
Mitochondrial trifunctional protein deficiency
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Multiple sulfatase deficiency
N-acetylglutamate synthase deficiency
Nemaline myopathy
Nephronophthisis
Netherton syndrome
Neuronal ceroid lipofuscinosis
Nezelof syndrome
Niemann-Pick disease, type C
Niemann-pick diseases
Ochronosis
Oculodentodigital syndrome
Oguchi disease
Omenn syndrome
Ornithine translocase deficiency
Orotic aciduria
Otospondyl- omegaepiphyseal dysplasia
Papillon–Lefèvre syndrome
Pendred syndrome
Persistent Mullerian duct syndrome
Phenylketonuria
Phosphofructokinase deficiency
Primary carnitine deficiency
Primary ciliary dyskinesia
Progressive external ophthalmoplegia
Prolidase deficiency
Propionic acidemia
Pseudodominance
Pseudoxanthoma elasticum
Purine nucleoside phosphorylase deficiency
Pycnodysostosis
Pyruvate carboxylase deficiency
Rabson-Mendenhall syndrome
Raine syndrome
Rapadilino syndrome
Recessive multiple epiphyseal dysplasia
Renal dysplasia-limb defects syndrome
Renal-hepa- tic-pancreatic dysplasia
Reproductive compensation
Restrictive dermopathy
Richner Hanhart syndrome
Rothmund–Thomson syndrome
Rotor syndrome
Sabinas brittle hair syndrome
Saccharopinuria
Salla disease
Sandhoff disease
Sanfilippo syndrome
Sarcosinemia
Scheie syndrome
Short-chain acyl-coenzyme A dehydrogenase deficiency
Shwachman-Diamond syndrome
Sickle cell trait
Sickle-cell disease
Situs inversus
Sly syndrome
Smith-Lemli-Opitz syndrome
Succinic semialdehyde dehydrogenase deficiency
Sugarman syndrome
Survival motor neuron spinal muscular atrophy
Tangier disease
Tay-Sachs disease
Tetrahydrobiopterin deficiency
Thalassemia
Trimethylaminuria
Triosephosphate isomerase deficiency
Type I tyrosinemia
Type III tyrosinemia
Tyrosinemia
Tyrosinemia type II
Urbach–Wiethe disease
Urocanic aciduria
Usher syndrome
Vaso-occlusive crisis
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Vici syndrome
Weissenbac- her-Zweymüller syndrome
Werner syndrome
Wilson's disease
Wolcott-Rallison syndrome
Woodhouse-Sakati syndrome
Xeroderma pigmentosum
Yunis-Varon syndrome
ZAP70 deficiency
Zazam Sheriff Phillips syndrome
Zunich–Kaye syndrome
more...
Rare diseases
(22)
GM1 gangliosidoses
Cholesteryl ester storage disease
Tay-sachs disease, ab variant
Farber disease
GM2 gangliosidoses
GM2 gangliosidoses
Gangliosidoses
Multiple sulfatase deficiency
Sly syndrome
Aspartylgl- ucosaminuria
Sandhoff disease
Alpha-mannosidosis
Fabry's disease
Sarcosinemia
Kanzaki disease
Fucosidosis
Arylsulfatase A deficiency
Lipidoses
Glanzmann thrombasthenia
Adenosine deaminase deficiency
Niemann-pick diseases
Neuronal ceroid lipofuscinosis
Leukocyte adhesion deficiency
more...
Genetic disorders
(44)
Niemann-Pick disease, SMPD1-associated
Refractory anemia with ringed sideroblasts
Glycogen storage disease type iv
Kostmann syndrome
Cerebrotendineous xanthomatosis
Cerebrotendineous xanthomatosis
GM1 gangliosidoses
Cholesteryl ester storage disease
Tay-sachs disease, ab variant
Farber disease
GM2 gangliosidoses
Gangliosidoses
Multiple sulfatase deficiency
Galactose-- 1-phosphate uridylyltransferase galactosemia
Glutaric acidemia type 1
Sly syndrome
N-acetylglutamate synthase deficiency
Aspartylgl- ucosaminuria
Sandhoff disease
Essential fructosuria
Acatalasia
Fabry's disease
Pseudo-Hurler polydystrophy
Sarcosinemia
Kanzaki disease
Fucosidosis
Bare lymphocyte syndrome
Carbamoyl phosphate synthetase I deficiency
Cystathioninuria
Glycogen storage disease type iii
Scheie syndrome
Arylsulfatase A deficiency
Lipidoses
Lecithin cholesterol acyltransferase deficiency
Cartilage hair hypoplasia
Glanzmann thrombasthenia
Adenosine deaminase deficiency
Lucey-Driscoll syndrome
Histidinemia
3 methylcrotonyl-coa carboxylase deficiency
Niemann-pick diseases
Hurler-Scheie Syndrome
Leukocyte adhesion deficiency
Abetalipop- roteinemia
Batten disease
more...
Diseases and disorders
(25)
Fructose bisphosphatase deficiency
Lymphohistiocytosis
Maroteaux-Lamy syndrome
Santavuori disease
Lipoprotein lipase deficiency
Lipoprotein lipase deficiency
Cerebrotendineous xanthomatosis
GM1 gangliosidoses
Farber disease
GM2 gangliosidoses
Gangliosidoses
Multiple sulfatase deficiency
Mucolipidosis I
Sandhoff disease
Fabry's disease
Fucosidosis
Refractory anemia with ringed sideroblasts
Arylsulfatase A deficiency
Lipidoses
Lecithin cholesterol acyltransferase deficiency
Cartilage hair hypoplasia
Lucey-Driscoll syndrome
Disorders of calcium metabolism
Kostmann syndrome
Niemann-pick diseases
Neuronal ceroid lipofuscinosis
more...
Medical condition
(62)
Jansky-bielschowsky disease
Sea-blue histiocyte syndrome
Familial xanthomatosis
Sphingolipidoses
Acute biphenotypic leukemia
Acute biphenotypic leukemia
Brown tendon sheath syndrome
Common bile duct cyst
Cranial nerve ix diseases
Cranial nerve vii diseases
Intrauterine cross-transfusion
Melanocytic vestibular schwannoma
Ninth cranial nerve diseases
Parietal region trauma
Piriformin syndrome
Post-traumatic tic disorder
Second cranial nerve diseases
Temporal region trauma
Reticular dysgenesis
Facial recognition agnosia
Senior health issues sensory agnosia
Somatotropin hypersecretion syndrome
Ocular retraction syndrome
Paraneoplastic autonomic dysfunction
Esophagopharyngeal diverticulum
Herpetic facial paralysis
Tracheal cyst
Pentosuria
Plasma cell leukemia
Fatty acid oxidation disorders
Amyloidosis, familial
Agnogenic myeloid metaplasia
Cerebrotendineous xanthomatosis
Cholesteryl ester storage disease
Farber disease
Mucolipidosis I
Galactose-- 1-phosphate uridylyltransferase galactosemia
Lysosomal storage diseases
Sly syndrome
Aspartylgl- ucosaminuria
Lymphohistiocytosis
Sandhoff disease
Essential fructosuria
Acatalasia
Fabry's disease
Sarcosinemia
Kanzaki disease
Fucosidosis
Bare lymphocyte syndrome
Carbamoyl phosphate synthetase I deficiency
Refractory anemia with ringed sideroblasts
Glycogen storage disease type iv
Scheie syndrome
Arylsulfatase A deficiency
Glanzmann thrombasthenia
Adenosine deaminase deficiency
Histidinemia
Hurler-Scheie Syndrome
Neuronal ceroid lipofuscinosis
Leukodystrophy
Lipoprotein lipase deficiency
Abetalipop- roteinemia
Batten disease
more...
Hydrolases
Human pancreatic lipase
Endothelial lipase
Beta-hexosaminidase A
Alpha/beta hydrolase fold
See also
(11)
Acid lipase
Mixed disorder of acid-base balance
Hyperchole- sterolemia, familial
Lysosomal
Refractory anemia with excess blasts in transformation
Refractory anemia with excess blasts in transformation
Glycolipid
Juvenile Myelomonocytic Leukemia (JMML)
Ashkenazi Jews topics
Hematopoietic stem cell transplantation
Angiokeratomas
Moshe Wolman
more...
more categories...
Health Providers & Organizations
›
Vitals.com
