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Deficiency Disease
Deficiency disease
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Malnutrition
(54)
Beriberi
Copper deficiency
Folate deficiency
Hypervitaminosis a
Iodine deficiency
Iodine deficiency
Iron deficiency (medicine)
Iron deficiency anemia
Pellagra
Vitamin C deficiency
Auxology
BP-5 Compact Food
Bill Emerson Good Samaritan Act of 1996
Child poverty
Chromium deficiency
Coeliac disease
Emaciation
Endemic goitre
F-100 (food)
Famine food
Famine relief
Famine response
Fluorine deficiency
Food and Agriculture Organization
Food desert
Hunger Plan
Hypovitaminosis A
Iodine deficiency in China
Korsakoff's syndrome
Kwashiorkor
Magnesium deficiency (medicine)
Manganese deficiency (medicine)
Marasmus
Meds and Food for Kids
Microvillous inclusion disease
Morning sickness
Muesli Belt
Nonne–Milroy–Meige syndrome
NutritionDay
Nutritional deficiencies
Omegaven
Overnutrition
Plumpy'nut
Rabbit starvation
Rachitic rosary
Rickets
Short bowel syndrome
Starvation
Starvation mode
Stunted growth
Superior mesenteric artery syndrome
Tropical sprue
Vitamin B6 excess
Walk the World
World Food Programme
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Immune system disorders
Immune deficiency disease
22q11.2 deletion syndrome
Zap70 deficiency
Wiskott-aldrich syndrome
Inborn errors of metabolism
(107)
Acid maltase deficiency
Adenosine deaminase deficiency
Galactosemia
Globoid cell leukodystrophy
Glucose-6-- phosphatase deficiency
Glucose-6-- phosphatase deficiency
Glycogen storage disease
Lecithin cholesterol acyltransferase deficiency
Lipidosis
Lysosomal storage diseases
McArdle disease
Ornithine carbamoylt- ransferase deficiency disease
Tangier disease
Wolman disease
2,4 Dienoyl-CoA reductase deficiency
2-Methylbutyryl-CoA dehydrogenase deficiency
3-Methylcr- otonyl-CoA carboxylase deficiency
3-hydroxy-- 3-methylglutaryl-CoA lyase deficiency
3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Acatalasia
Acid lipase disease
Adenylosuccinate lyase deficiency
Aldolase A deficiency
Analbuminaemia
Arakawa's syndrome II
Argininemia
Argininosuccinic aciduria
Aspartylgl- ucosaminuria
Beta-ketothiolase deficiency
Carbamoyl phosphate synthetase I 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
Essential fructosuria
Fucosidosis
Fumarase deficiency
Galactose-- 1-phosphate uridylyltransferase galactosemia
Glucose-galactose malabsorption
Glutaric acidemia type 2
Glutaric aciduria type 1
Glycogen storage disease type III
Guanidinoacetate methyltransferase deficiency
Hawkinsinuria
Hereditary fructose intolerance
Histidinemia
Holocarboxylase synthetase deficiency
Hyperlysinemia
Hypermethioninemia
Hyperprolinemia
Hypervalinemia
Idiosyncrasy
Inborn error of lipid metabolism
Inborn error of metabolism
Isobutyryl-coenzyme A dehydrogenase deficiency
Isovaleric acidemia
Lesch–Nyhan syndrome
Lipid storage disorders
Long-chain 3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Lysinuric protein intolerance
Lysosomal storage disease
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
N-Acetylglutamate synthase deficiency
Newborn screening
Niemann-Pick disease, type C
Organic acidemia
Ornithine translocase deficiency
Phenylketonuria
Primary carnitine deficiency
Prolidase deficiency
Propionic acidemia
Pyruvate carboxylase deficiency
Pyruvate kinase deficiency
Refsum's disease
Rotor syndrome
Sarcosinemia
Schindler disease
Short-chain acyl-coenzyme A dehydrogenase deficiency
Sly syndrome
Smith-Lemli-Opitz syndrome
Succinic semialdehyde dehydrogenase deficiency
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
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Iron metabolism
(31)
Aceruloplasminemia
African iron overload
Atransferrinemia
Iron overload disorder
Ceruloplasmin
Ceruloplasmin
Ferritin
Ferroportin
HFE hereditary hemochromatosis
Haemochromatosis type 3
Hemojuvelin
Hemoproteins
Hemosiderin
Hemosiderosis
Hepcidin
Hephaestin
Human iron metabolism
Iron deficiency (medicine)
Iron deficiency anemia
Iron metabolism disorder
Iron tests
Iron-binding proteins
Juvenile hemochromatosis
Neonatal hemochromatosis
Serum iron
Siderosis
TFR2
TFRC
Total iron-binding capacity
Transferrin
Transferrin receptor
Transferrin saturation
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Genetic disorder
(8)
Purine nucleoside phosphorylase deficiency
Phosphofructokinase deficiency
Factor xi deficiency
Albright's hereditary osteodystrophy
Aceruloplasminemia
Aceruloplasminemia
Adenosine deaminase deficiency
African iron overload
Zap70 deficiency
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Hepatology
Gaucher disease
Alpha 1 antitrypsin deficiency
Aceruloplasminemia
Acid maltase deficiency
Glycogen storage disease
Glucose-6-- phosphatase deficiency
Lysosomal storage diseases
(40)
Canavan disease
Fabry disease
Niemann Pick disease
Acid maltase deficiency
Alpha-mannosidosis
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Cholesteryl ester storage disease
Cystinosis
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher disease
Globoid cell leukodystrophy
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Lipidosis
Lysosomal storage disease
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
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
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Rare diseases
(15)
Alexander disease
Hartnup disease
WHIM syndrome
Acid maltase deficiency
Adenosine deaminase deficiency
Adenosine deaminase deficiency
Atransferrinemia
Wolman disease
Purine nucleoside phosphorylase deficiency
Fabry disease
Globoid cell leukodystrophy
Niemann Pick disease
Lipidosis
Gaucher disease
Zap70 deficiency
Wiskott-aldrich syndrome
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Immunodeficiency
(14)
Complement deficiency
Nezelof syndrome
Primary immune deficiency
X-scid
Adenosine deaminase deficiency
Adenosine deaminase deficiency
Bare lymphocyte syndrome
Common variable immunodeficiency
HIV
HIV/AIDS
ICF syndrome
Idiopathic CD4+ lymphocytopenia
Immunodeficiency (Acquired immunodeficiency)
Severe combined immunodeficiency
Severe combined immunodeficiency (non-human)
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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
Gangliosidosis
Gaucher disease
Globoid cell leukodystrophy
Glycogen storage disease type 0
Hereditary fructose intolerance
Homocystinuria
Hyperglycemia
Hyperinsulinemic hypoglycemia
Hyperinsulinism
Hypoglycemia
Inborn errors of metabolism
Ketotic hypoglycemia
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
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
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Blood disorders
Hematological malignancy
Christmas disease
Atransferrinemia
Factor xi deficiency
Wiskott-aldrich syndrome
Noninfectious immunodeficiency-related cutaneous conditions
(26)
22q11.2 deletion syndrome
Bare lymphocyte syndrome
Cartilage–hair hypoplasia
Chediak–Higashi syndrome
Chronic granulomatous disease
Chronic granulomatous disease
Common variable immunodeficiency
Complement deficiency
Graft-versus-host disease
Griscelli syndrome
Hyperimmunoglobulin E syndrome
Immunodeficiency with hyper-immu- noglobulin M
Immunoglobulin M deficiency
Leukocyte adhesion molecule deficiency
Myeloperoxidase deficiency
Neutropenia
Nezelof syndrome
Omenn syndrome
Purine nucleoside phosphorylase deficiency
Selective immunoglobulin A deficiency
Severe combined immunodeficiency
Thymoma with immunodeficiency
WHIM syndrome
Wiskott-aldrich syndrome
X-linked agammaglobulinemia
X-linked hyper-immu- noglobulin M syndrome
X-linked lymphoproliferative disease
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Nutrition disorder
Keshan disease
Hers' Disease
Biotin deficiency
Albright's hereditary osteodystrophy
EC number
Myophosphorylase
Glycogen debranching enzyme
Hexosaminidase A
Acid maltase
Genetic disorders
(39)
Abetalipop- roteinemia
Aicardi syndrome
Barth syndrome
Ornithine carbamoylt- ransferase deficiency disease
Aceruloplasminemia
Aceruloplasminemia
Acid maltase deficiency
Adenosine deaminase deficiency
22q11.2 deletion syndrome
Hyper IgM syndrome
McArdle disease
Acrodermatitis enteropathica
Adrenoleuk- odystrophy
Atransferrinemia
Glucose-6-- phosphatase deficiency
Wolman disease
Purine nucleoside phosphorylase deficiency
Tangier disease
Phosphofructokinase deficiency
Fabry disease
Globoid cell leukodystrophy
Niemann Pick disease
Lipidosis
Gaucher disease
Ataxia telangiectasia
Factor xi deficiency
Alexander disease
African iron overload
Alport syndrome
Hartnup disease
Canavan disease
Zap70 deficiency
Albright's hereditary osteodystrophy
Alpha 1 antitrypsin deficiency
Nezelof syndrome
Wiskott-aldrich syndrome
X-scid
WHIM syndrome
Lecithin cholesterol acyltransferase deficiency
Galactosemia
more...
Nutritional deficiencies
(21)
Ariboflavinosis
Pyridoxine deficiency
Selenium deficiency
Vitamin B12 Deficiency
Acrodermatitis enteropathica
Acrodermatitis enteropathica
Beriberi
Biotin deficiency
Boron deficiency (medicine)
Essential fatty acid deficiency
Folate deficiency
Iodine deficiency
Iron deficiency (medicine)
Kashin-Beck disease
Kwashiorkor
Marasmus
Pellagra
Protein-energy malnutrition
Vitamin A deficiency
Vitamin C deficiency
Vitamin K deficiency
Zinc deficiency
more...
Diseases and disorders
(58)
Adiposis dolorosa
Avitaminosis
Immunoproliferative
Sphingolipidoses
Factor ix deficiency
Factor ix deficiency
Complement 2 deficiency
Catabolysis
Milk-alkali syndrome
Peroxisomal disorders
Magnesium deficiency
Ornithine carbamoylt- ransferase deficiency disease
Aceruloplasminemia
Acid maltase deficiency
Adenosine deaminase deficiency
22q11.2 deletion syndrome
Hyper IgM syndrome
Glycogen storage disease
Acrodermatitis enteropathica
Atransferrinemia
Abetalipop- roteinemia
Beriberi
Iodine deficiency
Wolman disease
Purine nucleoside phosphorylase deficiency
Keshan disease
Pellagra
Tangier disease
Phosphofructokinase deficiency
Fabry disease
Lysosomal storage diseases
Christmas disease
Globoid cell leukodystrophy
Iron overload disorder
Niemann Pick disease
Vitamin C deficiency
Lipidosis
Gaucher disease
Ataxia telangiectasia
Factor xi deficiency
Alexander disease
African iron overload
Alport syndrome
Complement deficiency
Hartnup disease
Canavan disease
Hypervitaminosis a
Zap70 deficiency
Albright's hereditary osteodystrophy
Vitamin B12 Deficiency
Alpha 1 antitrypsin deficiency
Barth syndrome
Nezelof syndrome
Wiskott-aldrich syndrome
Pyridoxine deficiency
Lecithin cholesterol acyltransferase deficiency
Hypolipoproteinemia
Galactosemia
Iron deficiency anemia
more...
See also
(20)
Hyper IgM syndrome
Acrodermatitis enteropathica
Adrenoleuk- odystrophy
Enzymes
Pseudopseu- dohypopara- thyroidism
Pseudopseu- dohypoparathyroidism
Hypervitaminosis D
Vitamin B-7
Acyl CoA dehydrogenase
Tarui
Vitamin d deficiency
Metastatic calcification
Vitamin k deficiency
Acid alpha-glucosidase
Hyper IgM Syndrome Type 1
X linked
Vitamin B-9
Angiokeratomas
Mike Spencer
Ataxia telangiectasia
Obesity hypoventilation syndrome
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