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'Niemann Pick Diseases'
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Niemann Pick Diseases
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Topics Related to Niemann Pick Diseases
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Lipid storage disorders
(14)
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Gangliosidoses
Gangliosidoses
Gaucher disease
Leukodystrophy, globoid cell
Multiple sulfatase deficiency
Niemann Pick disease
Sandhoff disease
Wolman disease
Niemann-Pick disease, type C
Schindler disease
Tay-Sachs disease
more...
Metabolic disorders
(60)
Galactosemias
Activated protein C resistance
Adenosine deaminase deficiency
Albinism
Alcohol flush reaction
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
Disorders of calcium metabolism
Ectopic calcification
Farber disease
Fructose malabsorption
GM1 gangliosidoses
GM2 gangliosidoses
Galactosemic cataract
Gangliosidoses
Gaucher disease
Glycogen storage disease type 0
Hereditary fructose intolerance
Homocystinuria
Hyperglycemia
Hyperinsulinemic hypoglycemia
Hyperinsulinism
Hypoglycemia
Inborn errors of metabolism
Ketotic hypoglycemia
Lactose intolerance
Leukodystrophy, globoid cell
Lipid storage disorders
List of causes of hypoglycemia
Metab-L
Methemoglobinemia
Neuronal ceroid lipofuscinosis
Niemann Pick disease
Niemann-Pick disease, type C
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...
Skin conditions resulting from errors in metabolism
(87)
Adrenoleuk- odystrophy
Cerebrotendineous xanthomatosis
Fucosidosis
Hurler-Scheie Syndrome
Sialidosis
Sialidosis
Acute intermittent porphyria
Alkaptonuria
Amyloid purpura
Amyloidosis
Apolipoprotein B deficiency
B-mannosidase deficiency
CADASIL syndrome
Calcinosis cutis
Carotenosis
Citrullinemia
Combined hyperlipidemia
Diabetic bulla
Diabetic cheiroarthropathy
Diabetic dermadrome
Diabetic dermopathy
Dystrophic calcinosis cutis
Eruptive xanthoma
Erythropoietic porphyria
Erythropoietic protoporphyria
Fabry disease
Familial apoprotein CII deficiency
Familial dysbetalip- oproteinemia
Familial hypertrigl- yceridemia
Farber disease
Gaucher disease
Gout
Gunther disease
Hartnup disease
Hepatoeryt- hropoietic porphyria
Hereditary coproporphyria
Heredofamilial amyloidosis
Hunter syndrome
Hyaluronidase deficiency
Iatrogenic calcinosis cutis
Idiopathic scrotal calcinosis
Lafora disease
Lesch–Nyhan syndrome
Lichen amyloidosis
Limited joint mobility
Lipoprotein lipase deficiency
Macular amyloidosis
Medication-induced hyperlipop- roteinemia
Metastatic calcinosis cutis
Morquio syndrome
Myxedema
Necrobiosis lipoidica
Niemann Pick disease
Nodular amyloidosis
Nodular xanthoma
Normolipop- roteinemic xanthomatosis
Ochronosis
Osteoma cutis
Palmar xanthoma
Phenylketonuria
Porphyria
Porphyria cutanea tarda
Primary cutaneous amyloidosis
Primary systemic amyloidosis
Prolidase deficiency
Pseudoporphyria
Secondary cutaneous amyloidosis
Secondary systemic amyloidosis
Sitosterolemia
Subepidermal calcified nodule
Tangier disease
Transient erythroporphyria of infancy
Traumatic calcinosis cutis
Tuberoeruptive xanthoma
Tumoral calcinosis
Urbach–Wiethe disease
Variegate porphyria
Verruciform xanthoma
Waxy skin
Xanthelasma
Xanthoma
Xanthoma diabeticorum
Xanthoma planum
Xanthoma striatum palmare
Xanthoma tendinosum
Xanthoma tuberosum
Xanthomatosis
Xanthomatous biliary cirrhosis
more...
Autosomal recessive disorders
(20)
Tay-sachs disease, ab variant
Sly syndrome
Lipidosis
Metachromatic leukodystrophy
Mucolipidosis type IV
Mucolipidosis type IV
Bloom syndrome
Canavan disease
Batten disease
Familial dysautonomia
Niemann Pick disease
Leukodystrophy, globoid cell
Cerebrotendineous xanthomatosis
Wolman disease
Farber disease
Gangliosidoses
Multiple sulfatase deficiency
Sandhoff disease
Hurler-Scheie Syndrome
Fucosidosis
Gaucher disease
more...
Ashkenazi Jews topics
Niemann Pick disease
GM2 gangliosidoses
Mucolipidosis type IV
Bloom syndrome
Canavan disease
Gaucher disease
Familial dysautonomia
Rare diseases
(18)
Cholesteryl ester storage disease
Niemann Pick disease
Tay-sachs disease, ab variant
Leukodystrophy, globoid cell
Wolman disease
Wolman disease
Sly syndrome
GM1 gangliosidoses
Farber disease
Gangliosidoses
Multiple sulfatase deficiency
Lipidosis
GM2 gangliosidoses
Metachromatic leukodystrophy
Sandhoff disease
Bloom syndrome
Fucosidosis
Gaucher disease
Fabry disease
more...
Lysosomal storage diseases
(40)
Mucolipidosis II
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Canavan disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidoses
Gaucher disease
Glycogen storage disease type II
Glycoproteinosis
Hunter syndrome
Hurler-Scheie Syndrome
Leukodystrophy, globoid cell
Lipidosis
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...
Genetic disorders
(31)
Niemann-Pick disease, SMPD1-associated
Hyperostosis, cortical, congenital
Hereditary sensory and autonomic neuropathies
Jansky-bielschowsky disease
Refractory anemia with ringed sideroblasts
Refractory anemia with ringed sideroblasts
Genetic diseases
Niemann Pick disease
Tay-sachs disease, ab variant
Leukodystrophy, globoid cell
Cerebrotendineous xanthomatosis
Adrenoleuk- odystrophy
Wolman disease
Sly syndrome
GM1 gangliosidoses
Farber disease
Gangliosidoses
Galactosemias
Multiple sulfatase deficiency
Lipidosis
GM2 gangliosidoses
Cholesteryl ester storage disease
Metachromatic leukodystrophy
Sandhoff disease
Mucolipidosis type IV
Hurler-Scheie Syndrome
Bloom syndrome
Canavan disease
Fucosidosis
Batten disease
Gaucher disease
Fabry disease
more...
Diseases and disorders
(85)
Pick Disease
Sea-blue histiocyte syndrome
Acute biphenotypic leukemia
Reticular dysgenesis
Lymphohistiocytosis
Lymphohistiocytosis
Histiocytosis non-langerhans-cell
Sphingolipidoses
Glossopharyngeal nerve diseases
Type i complex regional pain syndrome
Myopathies, structural, congenital
Purpura, schoenlein-henoch
Enterocolitis, pseudomembranous
Fetofetal transfusion
Nakamura osame syndrome
Nanism due to growth hormone combined deficiency
Narrow oral fissure short stature cone shaped epiphyses
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
Lupus erythematosus, cutaneous
Cataplexy
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Physiologic nystagmus
N-acetyl-g- lucosamine-6-sulfate sulfatase deficiency
Intervertebral disk displacement
Rosenthal syndrome
Brachial plexus neuropathies
Leukemia
Optic neuropathy, ischemic
Neuroectodermal tumors primitive
Myelofibrosis
Maroteaux-Lamy syndrome
Nevus
Metabolic diseases
Niemann Pick disease
Leukodystrophy, globoid cell
Hyperostosis, cortical, congenital
Cerebrotendineous xanthomatosis
Lysosomal storage diseases
Wolman disease
Sly syndrome
Hereditary sensory and autonomic neuropathies
GM1 gangliosidoses
Farber disease
Gangliosidoses
Galactosemias
Multiple sulfatase deficiency
Jansky-bielschowsky disease
Lipidosis
Refractory anemia with ringed sideroblasts
GM2 gangliosidoses
Cholesteryl ester storage disease
Metachromatic leukodystrophy
Sandhoff disease
Mucolipidosis type IV
Hurler-Scheie Syndrome
Bloom syndrome
Canavan disease
Rare diseases
Fucosidosis
Sialidosis
Batten disease
Gaucher disease
Familial dysautonomia
Fabry disease
more...
Leukodystrophies
Adrenoleuk- odystrophy
Alexander disease
Canavan disease
Leukodystrophy, globoid cell
Metachromatic leukodystrophy
Pelizaeus-- Merzbacher disease
Zellweger syndrome
See also
(20)
Niemann-pick disease type d
Sphingomyelin
Refractory anemia with excess blasts in transformation
Juvenile Myelomonocytic Leukemia (JMML)
Lysosomal
Lysosomal
Gaze palsy
Enzyme
Mental retardation
The International League of Dermatological Societies
Www.nnpdf.org
Albert Niemann (paediatrician)
Hepatosplenomegaly
Spleen
Cord blood bank
Miglustat
Brain natriuretic peptide
Brain diseases
Liver biopsy
Bone marrow transplantation
Cholesterol
more...
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