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Niemann-pick Disease, Smpd1-associated
Niemann-Pick disease, SMPD1-associated
Overview
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Genetic disorders
(16)
Tay-sachs disease, ab variant
Cerebrotendineous xanthomatosis
GM1 gangliosidoses
GM2 gangliosidoses
Cholesteryl ester storage disease
Cholesteryl ester storage disease
Farber disease
Multiple sulfatase deficiency
Gangliosidoses
Fabry's disease
Batten disease
Niemann Pick disease
Wolman disease
Sandhoff disease
Metachromatic leukodystrophy
Krabbe disease
Spinocerebellar ataxia
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Autosomal recessive disorders
(12)
Neuronal ceroid lipofuscinosis
Tay-sachs disease, ab variant
Cerebrotendineous xanthomatosis
Farber disease
Multiple sulfatase deficiency
Multiple sulfatase deficiency
Gangliosidoses
Batten disease
Niemann Pick disease
Wolman disease
Sandhoff disease
Metachromatic leukodystrophy
Krabbe disease
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Rare diseases
(14)
Tay-sachs disease, ab variant
GM1 gangliosidoses
GM2 gangliosidoses
Cholesteryl ester storage disease
Farber disease
Farber disease
Multiple sulfatase deficiency
Gangliosidoses
Fabry's disease
Niemann Pick disease
Wolman disease
Sandhoff disease
Metachromatic leukodystrophy
Neuronal ceroid lipofuscinosis
Krabbe disease
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Skin conditions resulting from errors in metabolism
Cerebrotendineous xanthomatosis
Farber disease
Fabry's disease
Niemann Pick disease
Lipid storage disorders
(14)
Fabry's disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Gangliosidoses
Gangliosidoses
Gaucher's disease
Krabbe disease
Multiple sulfatase deficiency
Niemann Pick disease
Niemann-Pick disease, type C
Sandhoff disease
Schindler disease
Tay-Sachs disease
Wolman disease
more...
Metabolic disorders
(59)
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
Niemann-Pick disease, type C
Obesity
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
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Inborn errors of metabolism
Lysosomal storage diseases
Lysosomal storage disease
Lipid storage disorders
Cholesteryl ester storage disease
Wolman disease
Krabbe disease
Lipids
Glycolipid
Sphingolipids
Ceramide
Medical condition
(14)
Sea-blue histiocyte syndrome
Jansky-bielschowsky disease
Sphingolipidoses
Cerebrotendineous xanthomatosis
Cholesteryl ester storage disease
Cholesteryl ester storage disease
Farber disease
Lysosomal storage diseases
Fabry's disease
Batten disease
Wolman disease
Sandhoff disease
Metachromatic leukodystrophy
Neuronal ceroid lipofuscinosis
Krabbe disease
more...
Lysosomal storage diseases
(40)
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage 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
Hunter syndrome
Hurler syndrome
I-cell disease
Krabbe disease
Lipid storage disorder
Lysosomal storage disease
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann Pick disease
Niemann-Pick disease, type C
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
more...
See also
(9)
Diseases and disorders
SMPD1
Enzymes
Proteins
Sphingomyelinase
Sphingomyelinase
Chemical substances
Autosomal recessive
PMID
Metabolism
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