serw-MX  [xml]  
 


    
 DeCS Categories

A04 Respiratory System .
A04.623 Pharynx .
A04.623.490 Hypopharynx .
A06 Endocrine System .
A06.407 Endocrine Glands .
A06.407.747 Pituitary Gland .
A06.688 Neurosecretory Systems .
A06.688.357 Hypothalamo-Hypophyseal System .
A06.688.357.750 Pituitary Gland .
A08 Nervous System .
A08.186 Central Nervous System .
A08.186.211 Brain .
A08.186.211.464 Limbic System .
A08.186.211.464.497 Hypothalamus .
A08.186.211.464.497.352 Hypothalamus, Middle .
A08.186.211.464.497.352.435 Hypothalamo-Hypophyseal System .
A08.186.211.464.497.352.435.500 Pituitary Gland .
A08.186.211.730 Prosencephalon .
A08.186.211.730.317 Diencephalon .
A08.186.211.730.317.357 Hypothalamus .
A08.186.211.730.317.357.352 Hypothalamus, Middle .
A08.186.211.730.317.357.352.435 Hypothalamo-Hypophyseal System .
A08.186.211.730.317.357.352.435.500 Pituitary Gland .
A08.713 Neurosecretory Systems .
A08.713.357 Hypothalamo-Hypophyseal System .
A08.713.357.750 Pituitary Gland .
A14 Stomatognathic System .
A14.724 Pharynx .
A14.724.490 Hypopharynx .
C05 Musculoskeletal Diseases .
C05.651 Muscular Diseases .
C05.651.701 Paralyses, Familial Periodic .
C05.651.701.450 Hypokalemic Periodic Paralysis .
C10 Nervous System Diseases .
C10.668 Neuromuscular Diseases .
C10.668.491 Muscular Diseases .
C10.668.491.650 Paralyses, Familial Periodic .
C10.668.491.650.450 Hypokalemic Periodic Paralysis .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.483 Hyperlipoproteinemia Type III .
C16.320.565.398.500 Hypolipoproteinemias .
C16.320.565.398.500.440 Hypobetalipoproteinemias .
C16.320.565.618 Metal Metabolism, Inborn Errors .
C16.320.565.618.711 Paralyses, Familial Periodic .
C16.320.565.618.711.550 Hypokalemic Periodic Paralysis .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.500 Dyslipidemias .
C18.452.584.500.500 Hyperlipidemias .
C18.452.584.500.500.644 Hyperlipoproteinemias .
C18.452.584.500.500.644.485 Hyperlipoproteinemia Type III .
C18.452.584.500.875 Hypolipoproteinemias .
C18.452.584.500.875.440 Hypobetalipoproteinemias .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.483 Hyperlipoproteinemia Type III .
C18.452.648.398.500 Hypolipoproteinemias .
C18.452.648.398.500.440 Hypobetalipoproteinemias .
C18.452.648.618 Metal Metabolism, Inborn Errors .
C18.452.648.618.711 Paralyses, Familial Periodic .
C18.452.648.618.711.550 Hypokalemic Periodic Paralysis .
D06 Hormones, Hormone Substitutes, and Hormone Antagonists .
D06.472 Hormones .
D06.472.699 Peptide Hormones .
D06.472.699.631 Pituitary Hormones .
D06.472.699.631.692 Pituitary Hormones, Posterior .
D06.472.699.631.692.781 Vasopressins .
D12 Amino Acids, Peptides, and Proteins .
D12.644 Peptides .
D12.644.400 Neuropeptides .
D12.644.400.900 Vasopressins .
D12.644.456 Oligopeptides .
D12.644.456.925 Vasopressins .
D12.644.548 Peptide Hormones .
D12.644.548.691 Pituitary Hormones .
D12.644.548.691.692 Pituitary Hormones, Posterior .
D12.644.548.691.692.781 Vasopressins .
D12.776 Proteins .
D12.776.631 Nerve Tissue Proteins .
D12.776.631.650 Neuropeptides .
D12.776.631.650.937 Vasopressins .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Vasopressins .
Pitressin .
Vasopressin .
Vasopressin (USP) .
beta Hypophamine .
Antidiuretic Hormones .
beta-Hypophamine .
Antidiuretic hormones released by the NEUROHYPOPHYSIS of all vertebrates (structure varies with species) to regulate water balance and OSMOLARITY. In general, vasopressin is a nonapeptide consisting of a six-amino-acid ring with a cysteine 1 to cysteine 6 disulfide bridge or an octapeptide containing a CYSTINE. All mammals have arginine vasopressin except the pig with a lysine at position 8. Vasopressin, a vasoconstrictor, acts on the KIDNEY COLLECTING DUCTS to increase water reabsorption, increase blood volume and blood pressure. .
1.00
 
Hypokalemic Periodic Paralysis .
HOKPP .
HYPOKPP .
HYPOPP .
Hypokalemic Periodic Paralysis, Familial .
Periodic Paralysis- Hypokalemic .
Westphall Disease .
Periodic Paralysis Hypokalemic .
Periodic Paralysis, Hypokalemic .
Periodic Paralysis- Hypokalemics .
Familial Hypokalemic Periodic Paralysis .
Paralysis, Hypokalemic Periodic .
Primary Hypokalemic Periodic Paralysis .
PRIMARY HYPOKALEMIC PERIODIC PARALYIS .
An autosomal dominant familial disorder characterized by recurrent episodes of skeletal muscle weakness associated with falls in serum potassium levels. The condition usually presents in the first or second decade of life with attacks of trunk and leg paresis during sleep or shortly after awakening. Symptoms may persist for hours to days and generally are precipitated by exercise or a meal high in carbohydrates. (Adams et al., Principles of Neurology, 6th ed, p1483) .
0.54
 
Hypobetalipoproteinemias .
Familial Hypobetalipoproteinemia .
Hypo beta Lipoproteinemia .
Hypobetalipoproteinemia .
Hypo beta Lipoproteinemias .
Conditions with abnormally low levels of BETA-LIPOPROTEINS (low density lipoproteins or LDL) in the blood. It is defined as LDL values equal to or less than the 5th percentile for the population. They include the autosomal dominant form involving mutation of the APOLIPOPROTEINS B gene, and the autosomal recessive form involving mutation of the microsomal triglyceride transfer protein. All are characterized by low LDL and dietary fat malabsorption. .
0.53
 
Hypopharynx .
Hypopharynges .
Hypopharynxes .
Laryngopharynges .
Laryngopharynxes .
Laryngopharynx .
The bottom portion of the pharynx situated below the OROPHARYNX and posterior to the LARYNX. The hypopharynx communicates with the larynx through the laryngeal inlet, and is also called laryngopharynx. .
0.53
 
Pituitary Gland .
Hypophyseal Infundibulum .
Hypophyseal Stalk .
Hypophysis Cerebri .
Infundibulum .
Cerebri, Hypophysis .
Cerebrus, Hypophysis .
Gland, Pituitary .
Glands, Pituitary .
Hypophyseal Stalks .
Hypophyses .
Hypophysis Cerebrus .
Infundibular Hypothalamus .
Infundibular Stalks .
Infundibulums .
Pituitary Glands .
Pituitary Stalks .
Stalk, Hypophyseal .
Stalk, Infundibular .
Stalks, Hypophyseal .
Stalks, Infundibular .
Hypophysis .
Pituitary Stalk .
Hypothalamus, Infundibular .
Infundibular Stalk .
Infundibular Stem .
Infundibulum (Hypophysis) .
Infundibulum, Hypophyseal .
Hypophysial Stalk .
A small, unpaired gland situated in the SELLA TURCICA. It is connected to the HYPOTHALAMUS by a short stalk which is called the INFUNDIBULUM. .
0.52
 
Hyperlipoproteinemia Type III .
Familial Dysbetalipoproteinemia .
Familial Hypercholesterolemia with Hyperlipemia .
Hyperlipoproteinemia, Broad-beta .
Hyperlipoproteinemia, Type III .
Broad-beta Hyperlipoproteinemia .
Hyperlipoproteinemia, Broad beta .
Hyperlipoproteinemias, Type III .
Type III Hyperlipoproteinemia .
Type III Hyperlipoproteinemias .
Broad Beta Disease .
Dysbetalipoproteinemia .
Dysbetalipoproteinemia, Familial .
An autosomal recessively inherited disorder characterized by the accumulation of intermediate-density lipoprotein (IDL or broad-beta-lipoprotein). IDL has a CHOLESTEROL to TRIGLYCERIDES ratio greater than that of VERY-LOW-DENSITY LIPOPROTEINS. This disorder is due to mutation of APOLIPOPROTEINS E, a receptor-binding component of VLDL and CHYLOMICRONS, resulting in their reduced clearance and high plasma levels of both cholesterol and triglycerides. .
0.49