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Symptoms » Polydipsia » Glossary
 

Glossary for Polydipsia

Medical terms related to Polydipsia or mentioned in this section include:

  • Abdominal symptoms: Symptoms affecting the abdomen or digestive tract
  • Aceruloplasminemia: A rare genetic disorder characterized by a lack of the protein ceruloplasmin in the blood resulting in a buildup of iron in the liver, brain and pancreas. This in turn causes diabetes and degeneration of the neural system causing tremors and walking abnormalities.
  • Acid-Base Imbalance: A disruption to the normal acid-base equilibrium in the body. There are four main groups of disorder involving an acid-base imbalance: respiratory acidosis or alkalosis and metabolic acidosis or alkalosis. Obviously the severity of symptoms is determined by the degree of imbalance.
  • Acromegaly: An abnormal enlargement of the limbs due to increased secretion of growth hormone after the cessation of puberty
  • Adrenal Cancer: A malignant cancer that develops in the adrenal gland. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormone is involved. Adrenal hormones made in the cortex (outer part of the gland) are aldosterone, corticosteroids and androgenic steroids. Adrenalin and noradrenalin are the hormones made in the medulla (central part of the adrenal gland).
  • Adrenal Cortex Neoplasms: A tumor that develops in the adrenal gland. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormone is involved. Adrenal hormones made in the cortex (outer part of the gland) are aldosterone, corticosteroids and androgenic steroids.
  • Adrenal adenoma, familial: A benign tumor that develops in the adrenal gland and tends to run in families. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormone is involved. Adrenal hormones made in the cortex (outer part of the gland) are aldosterone, corticosteroids and androgenic steroids . Adrenalin and noradrenalin are the hormones made in the medulla (central part of the adrenal gland).
  • Adrenal gland hyperfunction: Excessive activity of the adrenal gland which causes excessive production of one or more adrenal hormones (aldosterone, corticosteroids, androgenic steroids, epinephrine and norepinephrine). The increased adrenal gland activity may be caused by an adrenal gland tumor or by excessive stimulation of the gland. Pituitary hormones stimulate adrenal gland activity.
  • Adrenal incidentaloma: A tumor of the adrenal gland that is discovered incidentally while performing an imaging examination for reasons other than an adrenal tumor. The tumor may be asymptomatic or can causes excessive secretion of adrenal hormones and resulting symptoms. The tumor may also be malignant or benign.
  • Adrenocortical carcinoma: A condition which is characterized by malignancy which affects the adrenocortex.
  • Alsing syndrome: A rare syndrome characterized mainly by kidney problems, skeletal abnormalities and a hole in the coloboma of the eye.
  • Anorexia Nervosa: A disorder where a distorted sense of body image leads to self-starvation to the point of death in some cases.
  • Anxiety: Excessive worry, anxiety, or fear.
  • Apparent Mineralocorticoid Excess, type 2: A form of inherited high blood pressure that starts during early childhood. The condition is caused by a genetic defect which results in an inborn error of metabolism of peripheral cortisol. Type 2 causes similar symptoms to type 1 but the urinary steroid levels are different.
  • Apparent mineralocorticoid excess: A form of inherited high blood pressure that starts during early childhood. The condition results from a genetic defect which causes impaired metabolism of cortisol.
  • Atropine -- Teratogenic Agent: There is strong evidence to indicate that exposure to Atropine during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Bartter Syndrome: A rare genetic disorder of kidney metabolism characterized by reduced blood acidity and low potassium levels.
  • Bartter Syndrome type 4: Bartter syndrome is a rare disorder where abnormal kidney metabolism results in low blood acidity an potassium levels. Type 4 also involves sensorineural deafness.
  • Bartter Syndrome type 4A: Bartter syndrome is a rare disorder where abnormal kidney metabolism results in low blood acidity an potassium levels. Type 4A also involves sensorineural deafness.
  • Bartter Syndrome type 4B: Bartter syndrome is a rare disorder where abnormal kidney metabolism results in low blood acidity an potassium levels. Type 4B also involves sensorineural deafness.
  • Bartter's syndrome, antenatal type 1: A rare genetic kidney disorder that causes hypokalemia. A defect in the NKCC2 gene impairs the functioning of the Na-Cl cotransporter and leads to electrolyte imbalance. The rate of death is high prior to diagnosis.
  • Body symptoms: Symptoms affecting the entire body features.
  • Boichis syndrome: A rare syndrome involving nephronophthisis (progressive destruction of kidney tissue) from birth which leads to kidney failure and liver fibrosis.
  • Brain symptoms: Symptoms affecting the brain
  • Bumetanide -- Teratogenic Agent: There is strong evidence to indicate that exposure to Bumetanide during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Chemical poisoning -- Glaze: Glazes are used to put a shiny finish on various surfaces such as pottery. Glazes contain chemicals such as lead and zinc oxide which can cause serious symptoms if sufficient quantities are eaten. The chemicals cause damage to the gastrointestinal lining and the damage may continue for weeks after the poison was ingested. Death can result in severe cases. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chronic Kidney Disease: Long-term and generally irreversible disease of the kidneys due to infection, obstruction, congenital diseases or generalised diseases causing failure of the kidneys' normal functions.
  • Common symptoms: The most common symptoms
  • Conn's syndrome: An adrenal gland disorder where excess aldosterone hormone is produced resulting in symptoms such as headache, fatigue, nocturia and increased urine production. Also called primary hyperaldosteronism.
  • Cushing syndrome: A rare syndrome where excessive secretion of corticosteroids by the adrenal cortex leads to a variety of symptoms. Hormone-secreting adrenal or pituitary tumors are often the cause of the excessive corticosteroid secretion.
  • Cushing-like symptoms: Symptoms similar to those of Cushing's disease
  • Cyclic vomiting syndrome: recurrent attacks of intense nausea, vomiting, abdominal pain with or without headache/ migraine
  • DEND syndrome: An inherited disorder characterized by developmental delay, epilepsy and diabetes.
  • Dehydration: Loss and reduction in body water levels
  • Diabetes: Symptoms similar to those of diabetes
  • Diabetes Insipidus: A condition which is characterized by polyuria causing dehydration and resulting in great thirst
  • Diabetes Insipidus, Neurogenic: A disturbed water balance due to a deficiency of vasopressin (antidiuretic) hormone which causes excessive thirst and urination. Causes include autoimmune disease, malignancy, trauma, infection and blood vessel disease.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 1: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 1 is linked to a defect on chromosome 6p21.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 10: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 10 is linked to a defect on chromosome 10p15.1.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 11: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 11 is linked to a defect on chromosome 14q24.3-q31.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 12: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 12 is linked to a defect on chromosome 2q33.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 13: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 13 is linked to a defect on chromosome 2q34.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 15: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 15 is linked to a defect on chromosome 6q21.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 17: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 17 is linked to a defect on chromosome 10q25.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 18: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 18 is linked to a defect on chromosome 5q31.1-q33.1.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 19: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 19 is linked to a defect on chromosome 2q24.3.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 2: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 2 is linked to a defect on chromosome 11p15.5.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 20: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 20 is linked to a defect on chromosome 12q24.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 21: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 21 is linked to a defect on chromosome 6q25.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 22: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 22 is linked to a defect on chromosome 3p21.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 23: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 23 is linked to a defect on chromosome 4q27.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 24: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 24 is linked to a defect on chromosome 10q23.31.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 3: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 3 is linked to a defect on chromosome 15q26.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 4: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 4 is linked to a defect on chromosome 11q13.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 5: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 5 is linked to a defect on chromosome 6q25.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 6: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 6 is linked to a defect on chromosome 18q21.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 7: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 7 is linked to a defect on chromosome 2q31.
  • Diabetes Mellitus, Insulin-Dependent, Susceptibility to, 8: Insulin-dependent diabetes is a condition where the body is unable to produce its own insulin in sufficient quantities to regulate blood sugar levels. Researchers have discovered a number of genes which are linked to an increased risk of developing type 1 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 81 is linked to a defect on chromosome 6q25-q27.
  • Diabetes Mellitus, Noninsulin-Dependent, Susceptibility to, 1: Noninsulin-dependent diabetes (Type 2 diabetes) is a type of diabetes that doesn't respond to insulin but does tend to respond to dietary measures and diabetes medication. Researchers have discovered a number of genes which are linked to an increased risk of developing Type 2 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 1 is linked to a defect on chromosome 2q37.3.
  • Diabetes Mellitus, Noninsulin-Dependent, Susceptibility to, 2: Noninsulin-dependent diabetes (Type 2 diabetes) is a type of diabetes that doesn't respond to insulin but does tend to respond to dietary measures and diabetes medication. Researchers have discovered a number of genes which are linked to an increased risk of developing Type 2 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 2 is linked to a defect on chromosome 12q24.2.
  • Diabetes Mellitus, Noninsulin-Dependent, Susceptibility to, 3: Noninsulin-dependent diabetes (Type 2 diabetes) is a type of diabetes that doesn't respond to insulin but does tend to respond to dietary measures and diabetes medication. Researchers have discovered a number of genes which are linked to an increased risk of developing Type 2 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 3 is linked to a defect on chromosome 20q12-q13.1.
  • Diabetes Mellitus, Noninsulin-Dependent, Susceptibility to, 4: Noninsulin-dependent diabetes (Type 2 diabetes) is a type of diabetes that doesn't respond to insulin but does tend to respond to dietary measures and diabetes medication. Researchers have discovered a number of genes which are linked to an increased risk of developing Type 2 diabetes. The genetic anomaly alone is not enough to cause the disease but simply increases the risk. Type 4 is linked to a defect on chromosome 5q34-q35.2.
  • Diabetes insipidus: A condition which is characterized by polyuria causing dehydration and resulting in great thirst
  • Diabetes insipidus, diabetes mellitus, optic atrophy: A rare association of diabetes insipidus, diabetes mellitus, optic atrophy, and deafness.
  • Diabetes insipidus, nephrogenic type 2: A rare congenital condition where the kidney fails to respond to the antidiuretic hormone (arginine vasopressin), thus preventing reabsorption of water. This results in excessive urination and thirst. Type II is specifically caused by a defect in the AQP2 gene on chromosome 12q13.
  • Diabetes insipidus, nephrogenic, dominant type: A rare dominantly inherited, congenital condition where the kidney fails to respond to the antidiuretic hormone (arginine vasopressin), thus preventing reabsorption of water. This results in excessive urination and thirst. The condition is specifically caused by a defect in the AQP2 gene on chromosome 12q13.
  • Diabetes insipidus, nephrogenic, recessive type: A rare recessively inherited, congenital condition where the kidney fails to respond to the antidiuretic hormone (arginine vasopressin), thus preventing reabsorption of water. This results in excessive urination and thirst. The condition is specifically caused by a defect in the AQP2 gene on chromosome 12q13.
  • Diabetes mellitus, transient neonatal: A form of infant diabetes that starts usually in the month of life but then usually disappears within a year. The condition predisposes the infant to diabetes later in life.
  • Diabetes-like symptoms: Symptoms similar to those of diabetes
  • Diabetes-related symptoms: Symptoms similar to diabetes or closely related.
  • Diarrhea: Loose, soft, or watery stool.
  • Digestive symptoms: Any symptoms affecting the digestive tract.
  • Diuresis: increased production of urine by the kidney
  • East Syndrome: A rare syndrome characterized mainly by mental retardation, deafness, ataxia and electrolyte imbalance.
  • Electrolyte abnormality: An imbalance in the level of any of a number of chemicals (electrolytes) in the blood stream e.g. chloride, sodium, magnesium, potassium, calcium, phosphate and bicarbonate. Symptoms can vary depending on which electrolyte is involved and the severity of the imbalance - severe cases can readily lead to death. An electrolyte abnormality can be caused by such things excessive loss of body fluid through vomiting or diarrhea, kidney conditions, malabsorption and various drugs such as diuretics and chemotherapy drugs.
  • Excessive sweating: A condition which is characterized by an abnormal excess of sweating
  • Excessive thirst in children: Excessive thirst in children is the experience of having considerable thirst in a child.
  • Familial hypopituitarism: Impaired pituitary gland hormone-producing activity that tends to run in families. The failure of the pituitary gland in turn affects other hormone-producing glands which rely on the hormones from the pituitary gland for their activity. Symptoms are determined by the degree and type of hormone deficiency involved.
  • Fanconi syndrome: Fanconi syndrome that occurs secondary to the accumulation of crystals of light-chain immunoglobulin molecules in the kidney tubules which affects their functioning.
  • Fever: Raised body temperature usually with other symptoms.
  • Froelich's syndrome: A rare condition where an endocrine abnormality (caused by such things as a pituitary tumor or damage to the hypothalamus) affects hormone levels which results in a variety of symptoms.
  • Gitelman syndrome: A rare, relatively mild, genetic kidney disorder that causes hypokalemia. The defective gene (NCCT) impairs the function of the Na-Cl cotransporter.
  • Glory lily poisoning: The glory lily is a type of vine which bears unusual yellow and red flowers. It is often used as an indoor and outdoor ornamental plant. The plant contains various chemicals that can cause serious symptoms if eaten. The roots are the most toxic part of the plant. The plant is considered very toxic and serious cases can result in death.
  • Glyburide -- Teratogenic Agent: There is evidence to indicate that exposure to Glyburide (an antidiabetic drug) during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Graves Disease: A condition which is an autoimmune disease that affects the thyroid resulting hyperthyroidism
  • Head injury: Any injury that occurs to the head
  • Head symptoms: Symptoms affecting the head or brain
  • Hydrochlorothiazide -- Teratogenic Agent: There is evidence to indicate that exposure to Hydrochlorothiazide during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Hyperadrenalism: Excessive levels of adrenal hormones in the body. Symptoms depend on which hormone is involved and the degree of involvement. Adrenal hormones are aldosterone, corticosteroids, androgenic steroids, epinephrine and norepinephrine.
  • Hypercalcemia: Raised blood calcium levels
  • Hyperglycemia: Where there is an increase above normal of the blood sugar levels
  • Hyperparathyroidism: Increased secretion of parathyroid hormone from the parathyroid glands.
  • Hyperparathyroidism, primary: A rare genetic disorder where excessive activity of the parathyroid gland causes increased blood calcium levels which can cause various problems.
  • Hypokalemia: Abnormally low levels of potassium in the blood.
  • Intermediate cystinosis: Cystinosis is a condition where excess amino acid cystine builds up to harmful levels in the body. The intermediate form of cystinosis starts later than the nephropathic form but the symptoms are the same.
  • Juvenile nephronophthisis: A rare inherited kidney disorder characterized by formation of cysts inside the kidney, kidney fibrosis and tubular atrophy which leads to progressive kidney failure.
  • Langerhans Cell Histiocytosis: A condition which is characterized by proliferation of Langerhans cells
  • Malnutrition-related diabetes mellitus: Diabetes mellitus that is caused by a chronic malnutrition state
  • Medullary cystic kidney disease, autosomal recessive: A genetic kidney disease which causes kidney failure in children, usually during adolescence.
  • Metformin -- Teratogenic Agent: There is evidence to indicate that exposure to Metformin during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Methacycline -- Teratogenic Agent: There is evidence to indicate that exposure to Methacycline during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Muscle symptoms: Symptoms affecting the muscles of the body
  • Musculoskeletal symptoms: Symptoms affecting muscles or bones of the skeleton.
  • Nephrogenic diabetes insipidus: A rare inherited condition where the kidneys can't concentrate the urine sufficiently which results in excessive urination and thirst. The condition occurs because the kidneys are unable to respond to the antidiuretic hormone.
  • Nephronophthisis 2: A genetic kidney disorder which causes kidney failure during childhood. Other problems such as underdeveloped lungs may also be associated with the condition. Type 2 is caused by a defect in the inversin gene.
  • Nephronophthisis 3: A genetic kidney disorder which causes kidney failure during adolescence. Other problems such as underdeveloped lungs may also be associated with the condition. Type 3 is caused by a defect in the NPHP3 gene.
  • Nephronophthisis 4: A genetic kidney disorder which causes kidney failure during adolescence. Other problems such as underdeveloped lungs may also be associated with the condition. Type 4 is caused by a defect in the NPHP4 gene.
  • Nephronophthisis 7: A genetic kidney disorder which causes kidney failure during adolescence. Other problems such as underdeveloped lungs may also be associated with the condition. Type 7 is caused by a defect in the GLIS2 gene.
  • Nephronophthisis familial, adult -- spastic quadriparesis: A very rare syndrome characterized mainly by progressive kidney destruction and spasticity and weakness of arms and legs.
  • Nephropathic cystinosis: Cystinosis is a condition where excess amino acid cystine builds up to harmful levels in the body. The nephropathic form of cystinosis usually starts during infancy and can result in severe complications if untreated.
  • Nerve symptoms: Symptoms affecting the nerves
  • Neurological symptoms: Any symptoms that are caused by neurological conditions
  • Neurosarcoidosis: A rare disorder involving sarcoidosis of the nervous system. Sarcoidosis is a chronic inflammatory disorder that can affect virtually any part of the body. Neurosarcoidosis involves inflammation and abnormal deposits in parts of the nervous system including the brain and spinal cord which affects their functioning. Symptoms may be sudden and severe or may be mild and progress slowly. Symptoms are determined by the degree of nerve involvement.
  • Numbness of both elbows: Numbness of both elbows refers to the loss or reduction of sensation in the elbows.
  • Oak poisoning: The oak is a large tree which has distinctive leaves and bears acorns. The acorns and young leaves contain chemicals (gallotannins, quercitrin and quercitin) which can cause symptoms if eaten. The plant is considered to have a low level of toxicity. The nuts are edible if the tannins have been leached out.
  • Oligomeganephronic renal hypoplasia: A congenital renal hypoplasia associated with chronic renal failure in children. Also called oligomeganephronia.
  • Pain: Any type of pain sensation symptoms.
  • Parathyroid cancer, adult: A rare cancer that can occur in the parathyroid gland in adults. The parathyroid glands regulate body calcium levels so cancer of the gland upsets the body's calcium balance causing muscle, bone and other symptoms.
  • Phenol sulfotransferase deficiency: A rare inherited disorder where the body is deficient in an enzyme (phenol sulfotransferase) which makes them unable to process phenols and other toxic substance in the body. A buildup of phenol in the body can cause physical and behavioral problems.
  • Polyuria: Excessive urination during pregnancy.
  • Primary Hyperaldosteronism: An adrenal gland disorder where excess aldosterone hormone is produced resulting in symptoms such as headache, fatigue, nocturia and increased urine production. Also called Conn's syndrome.
  • Primary tubular proximal acidosis: A rare disorder where abnormal function of the proximal kidney tubules causes a buildup of acid in the body. The kidney abnormality is not due to any other disease, condition or injury.
  • Proximal Renal Tubular Acidosis: This is a condition that is characterised by a metabolic acidosis state caused by impairment of a persons renal function
  • Renal disorder: disease affecting the kidneys
  • Schroeder syndrome 1: High blood pressure and reduced salt concentration in sweat associated with an overactive adrenal cortex which is involved with hormone production.
  • Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance: A rare syndrome characterized mainly by mental retardation, deafness, ataxia and electrolyte imbalance.
  • Sensations: Changes to sensations or the senses
  • Sensory symptoms: Symptoms affecting the sensory systems.
  • Sheehan Syndrome: A rare condition that occurs in women who suffer a severe uterine hemorrhage during childbirth. The resulting blood loss may damage the pituitary gland and result in hypopituitarism.
  • Sickle Cell Anemia: Sickle cell anemia is an inherited blood disorder characterized by red blood cells which are crescent-shaped rather than the normal doughnut shape. These abnormally shaped red blood cells are unable to function normally and tend to undergo premature destruction which leads to anemia. If the genetic defect which causes the condition is inherited from both parents the condition can be quite severe whereas if it is inherited from only one parent, often there are no symptoms. The abnormally shaped red blood cells can cause problems when they clump together and block blood vessels.
  • Sjogren's Syndrome: Autoimmune disease damaging the eye tear ducts and other glands.
  • Skin symptoms: Symptoms affecting the skin.
  • Stress: Emotional stress (sometimes refers to physical stress)
  • Systemic Capillary Leak Syndrome: A rare disease where episodes of leaking blood capillaries results in a rapid drop in blood pressure which can be life-threatening. Episodes usually last for a few days. The range and severity of symptoms experienced may range somewhat amongst patients.
  • Thirst: Inappropriate excessive thirst.
  • Thyrotoxicosis: hypermetabolic clinical syndrome resulting from serum elevations in thyroid hormone levels, specifically free thyroxine (T4), triiodothyronine (T3), or both.
  • Toxic mushrooms -- Renal toxic (orelline): Some mushrooms (Amanita smithiana) contain chemicals (allenic norleucine, chlorocrotyglycine) which can cause kidney damage.
  • Vasopressin-resistant diabetes insipidus: A condition which is characterised by normal renal filtration and solute excretion however there is a persistent hypotonic urine
  • Vomiting: Vomiting or retching symptoms.
  • Weakness: Symptoms causing weakness of the body
  • Wohlmann-Caglkar syndrome: A kidney abnormality that can occur in infants.
  • Wolfram Syndrome 2: Wolfram Syndrome is a condition characterized by the association of diabetes insipidus, diabetes mellitus, optic atrophy and deafness. Type 2 is the result of a genetic defect and is similar to type 1 but there is no diabetes insipidus and patients tend to develop gastrointestinal problems.

Conditions listing medical symptoms: Polydipsia:

The following list of conditions have 'Polydipsia' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

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