Deficiency disease

• 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
  • more...

• 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
  • more...

• 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
  • more...

• 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
  • more...

• 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
  • more...

• 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
  • more...

• 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)
  • 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
  • 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
  • more...

• 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
  • more...

• 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
  • more...

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