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Deficiency diseases in plants.   4
Deficiency diseases in plants -- Diagnosis.   2
Deficiency diseases in plants -- Periodicals : Journal of plant nutrition (Online)  1979- 1
Deficiency diseases -- Nutritional aspects -- Case studies. : Case studies in physiology and nutrition / Lynne Berdanier, Carolyn D. Berdanier  2010 1
Deficiency diseases -- Prevention. : Guidelines on food fortification with micronutrients / edited by Lindsay Allen ... [and others]  2006 1
Deficiency Diseases -- prevention & control.   6
Deficiency Diseases -- therapy. : Guidelines for the inpatient treatment of severely malnourished children / authors, Ann Ashworth [and others]  2003 1
Deficiency diseases -- Treatment -- Handbooks, manuals, etc. : Obstacles to cure : toxicity, deficiency & infection : a practitioner's manual / Jon Gamble  2010 1
Estrogens -- deficiency. : Estrogen versus cancer / Zsuzanna Suba  2009 1
 

Deficiency, F9 -- See Hemophilia B


A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008)
  1
 

Deficiency, Factor 11 -- See Factor XI Deficiency


A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting in a systemic blood-clotting defect called hemophilia C or Rosenthal's syndrome, that may resemble classical hemophilia
  1
 

Deficiency, Factor Eleven -- See Factor XI Deficiency


A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting in a systemic blood-clotting defect called hemophilia C or Rosenthal's syndrome, that may resemble classical hemophilia
  1
 

Deficiency, Factor IX -- See Hemophilia B


A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008)
  1
 

Deficiency, Factor VIII -- See Hemophilia A


The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage
  1
 

Deficiency, Factor XI -- See Factor XI Deficiency


A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting in a systemic blood-clotting defect called hemophilia C or Rosenthal's syndrome, that may resemble classical hemophilia
  1
Fatty Acids, Essential -- deficiency. : Essential fatty acids and eicosanoids : invited papers from the Third International Congress / editors, Andrew Sinclair, Robert Gibson  1992 1
 

Deficiency, Folic Acid -- See Folic Acid Deficiency


A nutritional condition produced by a deficiency of FOLIC ACID in the diet. Many plant and animal tissues contain folic acid, abundant in green leafy vegetables, yeast, liver, and mushrooms but destroyed by long-term cooking. Alcohol interferes with its intermediate metabolism and absorption. Folic acid deficiency may develop in long-term anticonvulsant therapy or with use of oral contraceptives. This deficiency causes anemia, macrocytic anemia, and megaloblastic anemia. It is indistinguishable from vitamin B 12 deficiency in peripheral blood and bone marrow findings, but the neurologic lesions seen in B 12 deficiency do not occur. (Merck Manual, 16th ed)
  1
 

Deficiency, GBA -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
  1
 

Deficiency, GLA -- See Fabry Disease


An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders
  1
 

Deficiency, Glucocerebrosidase -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
  1
Glutathione Peroxidase -- deficiency. : Selenium and male fertility / Matilde Maiorino  2016 1
Growth Substances -- deficiency. : Psychoneuroendocrinology : brain, behavior, and hormonal interactions / Clarissa S. Holmes, editor  1990 1
 

Deficiency, Hexosaminidase A -- See Tay-Sachs Disease


An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry
  1
 

Deficiency, Hexosaminidase alpha-Subunit (Variant B) -- See Tay-Sachs Disease


An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry
  1
Human Growth Hormone -- deficiency.   2
Iodine -- deficiency.   2
Iron -- deficiency.   7
 

Deficiency, Magnesium -- See Magnesium Deficiency


A nutritional condition produced by a deficiency of magnesium in the diet, characterized by anorexia, nausea, vomiting, lethargy, and weakness. Symptoms are paresthesias, muscle cramps, irritability, decreased attention span, and mental confusion, possibly requiring months to appear. Deficiency of body magnesium can exist even when serum values are normal. In addition, magnesium deficiency may be organ-selective, since certain tissues become deficient before others. (Harrison's Principles of Internal Medicine, 12th ed, p1936)
  1
Manganese -- deficiency. : Manganese in health and disease / edited by Dorothy J. Klimis-Tavantzis  1994 1
 

Deficiency, Mental -- See Intellectual Disability


Subnormal intellectual functioning which originates during the developmental period. This has multiple potential etiologies, including genetic defects and perinatal insults. Intelligence quotient (IQ) scores are commonly used to determine whether an individual has an intellectual disability. IQ scores between 70 and 79 are in the borderline range. Scores below 67 are in the disabled range. (from Joynt, Clinical Neurology, 1992, Ch55, p28)
  1
Micronutrients -- deficiency.   5
Nitric Oxide -- deficiency. : Pathophysiology and clinical applications of nitric oxide / edited by Gabor M. Rubanyi  1999 1
 

Deficiency, Ornithine Transcarbamylase -- See Ornithine Carbamoyltransferase Deficiency Disease


An inherited urea cycle disorder associated with deficiency of the enzyme ORNITHINE CARBAMOYLTRANSFERASE, transmitted as an X-linked trait and featuring elevations of amino acids and ammonia in the serum. Clinical features, which are more prominent in males, include seizures, behavioral alterations, episodic vomiting, lethargy, and coma. (Menkes, Textbook of Child Neurology, 5th ed, pp49-50)
  1
 

Deficiency, OTC -- See Ornithine Carbamoyltransferase Deficiency Disease


An inherited urea cycle disorder associated with deficiency of the enzyme ORNITHINE CARBAMOYLTRANSFERASE, transmitted as an X-linked trait and featuring elevations of amino acids and ammonia in the serum. Clinical features, which are more prominent in males, include seizures, behavioral alterations, episodic vomiting, lethargy, and coma. (Menkes, Textbook of Child Neurology, 5th ed, pp49-50)
  1
 

Deficiency, Oxidative Phosphorylation -- See Mitochondrial Diseases


Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes
  1
 

Deficiency, Oxygen -- See Hypoxia


Sub-optimal OXYGEN levels in the ambient air of living organisms
  1
 

Deficiency, Protein -- See Protein Deficiency


A nutritional condition produced by a deficiency of proteins in the diet, characterized by adaptive enzyme changes in the liver, increase in amino acid synthetases, and diminution of urea formation, thus conserving nitrogen and reducing its loss in the urine. Growth, immune response, repair, and production of enzymes and hormones are all impaired in severe protein deficiency. Protein deficiency may also arise in the face of adequate protein intake if the protein is of poor quality (i.e., the content of one or more amino acids is inadequate and thus becomes the limiting factor in protein utilization). (From Merck Manual, 16th ed; Harrison's Principles of Internal Medicine, 12th ed, p406)
  1
 

Deficiency, Proteostasis -- See Proteostasis Deficiencies


Disorders caused by imbalances in the PROTEIN HOMEOSTASIS network - synthesis, folding, and transport of proteins; post-translational modifications; and degradation or clearance of misfolded proteins
  1
Pyruvate Kinase -- deficiency. : Pyruvate kinase deficiency / Alberto Zanella  2016 1
 

Deficiency, Respiratory Chain -- See Mitochondrial Diseases


Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes
  1
 

Deficiency, Riboflavin -- See Riboflavin Deficiency


A dietary deficiency of riboflavin causing a syndrome chiefly marked by cheilitis, angular stomatitis, glossitis associated with a purplish red or magenta-colored tongue that may show fissures, corneal vascularization, dyssebacia, and anemia. (Dorland, 27th ed)
  1
Selenium -- deficiency. : Selenium : its molecular biology and role in human health / edited by Dolph L. Hatfield, Marla J. Berry, and Vadim N. Gladyshev  2006 1
Serpins -- deficiency. : Serpins and the serpinopathies / James Whisstock  2007 1
 

Deficiency, Smooth Pursuit -- See Ocular Motility Disorders


Disorders that feature impairment of eye movements as a primary manifestation of disease. These conditions may be divided into infranuclear, nuclear, and supranuclear disorders. Diseases of the eye muscles or oculomotor cranial nerves (III, IV, and VI) are considered infranuclear. Nuclear disorders are caused by disease of the oculomotor, trochlear, or abducens nuclei in the BRAIN STEM. Supranuclear disorders are produced by dysfunction of higher order sensory and motor systems that control eye movements, including neural networks in the CEREBRAL CORTEX; BASAL GANGLIA; CEREBELLUM; and BRAIN STEM. Ocular torticollis refers to a head tilt that is caused by an ocular misalignment. Opsoclonus refers to rapid, conjugate oscillations of the eyes in multiple directions, which may occur as a parainfectious or paraneoplastic condition (e.g., OPSOCLONUS-MYOCLONUS SYNDROME). (Adams et al., Principles of Neurology, 6th ed, p240)
  1
 

Deficiency Syndrome, Antibody -- See Immunologic Deficiency Syndromes


Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral
  1
 

Deficiency Syndrome, Immunologic -- See Immunologic Deficiency Syndromes


Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral
  1
 

Deficiency Syndrome, Immunological -- See Immunologic Deficiency Syndromes


Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral
  1
 

Deficiency Syndromes, Antibody -- See Immunologic Deficiency Syndromes


Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral
  1
 

Deficiency Syndromes, Immunologic -- See Immunologic Deficiency Syndromes


Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral
  1
 

Deficiency Syndromes, Immunological -- See Immunologic Deficiency Syndromes


Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral
  1
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