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Symptoms » Acidosis » Glossary
 

Glossary for Acidosis

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

  • 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency: A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Symptoms tend to be more severe in males who suffer progressive neurodegeneration whereas females tend to suffer mainly from developmental delay.
  • 3-alpha-hydroxyisobutyryl-CoA hydrolase deficiency: A metabolic disorder involving an enzyme deficiency which causes symptoms such as degeneration of the nervous system. The other features of the disorder are somewhat variable.
  • 3-methylglutaconic aciduria, type 4: A rare genetic disorder where the body's cells are unable to make sufficient energy resulting in an accumulation in the body of 3-methylglutaconic acid. Type 4 is characterized by symptoms which overlap type 1 and 3.
  • Abdominal symptoms: Symptoms affecting the abdomen or digestive tract
  • Abnormal blood test symptoms: Abnormal results from diagnostic blood tests.
  • Acidemia, propionic: An inherited genetic disorder where the body is incapable of processing some proteins and fats resulting in the accumulation of certain substances in the body which causes the symptoms of the condition. The condition can be life threatening.
  • Acidosis: The accumulation of hydrogen ions or the depletion of the alkaline reserve in the body.
  • Acute kidney failure: The sudden and acute loss of kidney function
  • Acute tubulointerstitial nephritis and uveitis syndrome: The association of a sudden kidney disorder with eye inflammation. Autoimmune processes are believed to be involved.
  • Alcohol -- Teratogenic Agent: There is strong evidence to indicate that exposure to Alcohol 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.
  • Alkalosis: A condition that iscaused by the accumulation of base in the body.
  • Anoxia: A condition marked by a lack of oxygen.
  • Apple seed poisoning: Apple seeds contain a toxic chemical called amygdalin which can cause serious symptoms if eaten in large quantities. Hospital admission is recommended if more than 50 apple seeds have been consumed.
  • Biotinidase deficiency: A metabolic disorder where the body lacks the enzyme biotinidase needed to process the vitamin called biotin (vitamin H) into carboxylase enzymes.
  • Blood symptoms: Symptoms affecting the blood and its blood cells.
  • Body symptoms: Symptoms affecting the entire body features.
  • Bright's Disease: A condition where the parts of the kidneys that are responsible for filtering become inflamed and results in blood and proteins accidentally leaking into the urine. The condition can occur after certain infections and serious kidney dysfunction can result in severe or chronic complications.
  • Cardiogenic shock: an inadequate circulation of blood due to primary failure of the ventricles of the heart to function effectively
  • Cardiomyopathy -- hypotonia -- lactic acidosis: A rare syndrome characterized by heart muscle disease, reduced muscle tone and lactic acidosis from birth.
  • Cataract and cardiomyopathy: A rare syndrome characterized by the association of congenital cataracts, heart muscle disease, lactic acidosis and skeletal muscle disease. The disorder involves the abnormal storage of lipids and glycogen in the skeletal and heart muscles. The cataracts progress rapidly and require surgery. The severity of the disorder ranges from stillbirth to survival into the fourth decade.
  • Chemical poisoning -- Endothall: Endothall is a chemical used mainly as a pesticide and rodenticide but it is rarely used today. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Strychnine: Strychnine is used as a rodenticide. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Cholera: An acute bacterial disease transmitted through food or water contaminated with human faeces. The intestinal infection is caused by the bacterium Vibrio cholerae.
  • Classic Distal Renal Tubular Acidosis: A condition which is characterized by the formation of an acidosis due to a problem with the renal distal tubule
  • Coenzyme Q cytochrome c reductase deficiency of: A rare genetic defect where an enzyme deficiency (CoQ-Cytochrome C reductase) disrupts cellular processes. Any of a variety of the components of the enzyme may be missing or defective and hence the clinical presentation and severity may vary. The deficiency may result in a variety of symptoms and conditions of variable severity such as cardiomyopathy, fatal infant conditions and Leber's myopathy.
  • Colibacillosis: Infection with a bacteria called Escherichia coli. Infection can cause severe diarrhea or septicemia. The bacteria can also produce toxins which can affect other parts of the body also. Infections can occur anywhere in the world but some developing countries have endemic areas. Transmission can occur contaminated animal products or contact with infected cats and dogs.
  • Complex 1 mitochondrial respiratory chain deficiency: A rare genetic defect where an enzyme deficiency (NADH CoQ) disrupts cellular processes and causes various organic acid disorders. Any of a variety of the components of the enzyme may be missing or defective and hence the clinical presentation and severity may vary. Presentation may range from infantile death to various disorders such as Leigh's disease, Parkinson's disease and cardiomyopathy.
  • Copperhead snake poisoning: The Copperhead snake is a poisonous snake found mainly in parts of North America. The toxicity of the poison varies among species but some species are extremely poisonous and readily result in death if the patient is not treated.
  • Crotalidae snake poisoning: Crotalids are snakes from the Crotalidae family. This group of snakes includes rattlesnakes which are usually found in America. These snakes are easily identified by the "rattle" at the tip of their tails. The toxicity of the venom can vary among species but some can result in death if prompt treatment is not given.
  • Cutler Syndrome: A rare disorder characterized by multisystem disorders including muscle wasting, ataxia, epilepsy, anemia and kidney disease. The kidney disease is most likely present at birth.
  • DEND syndrome: An inherited disorder characterized by developmental delay, epilepsy and diabetes.
  • DKA: A metabolic acidosis that results from the accumulation of ketones when diabetes mellitus is poorly controlled
  • 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-like symptoms: Symptoms similar to those of diabetes
  • Diabetic Ketoacidosis: A metabolic acidosis that results from the accumulation of ketones when diabetes mellitus is poorly controlled
  • Diabetic ketoacidosis: A metabolic acidosis that results from the accumulation of ketones when diabetes mellitus is poorly controlled
  • Fanconi renotubular syndrome: A condition where the kidneys are unable to reabsorb glucose and amino acids and hence they are excreted in the urine. The condition may be inherited or occur as a result of heavy metal toxicity, malignancy and myeloma.
  • 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.
  • Fanconi-ichthyosis-dysmorphism: A very rare syndrome characterized by scaly skin (ichthyosis), anemia, muscle anomalies and various other abnormalities. All six reported cases died within 6 months.
  • Finnish lethal neonatal metabolic syndrome: A very rare lethal metabolic disorder characterized by a deficiency of complex III which causes brain, kidney and liver problems and ultimately results in early death.
  • Fistula: The abnormal passage between two internal organs
  • Fructose-1,6-bisphosphatase deficiency, hereditary: A rare inherited condition where an enzyme deficiency (fructose-1,6-bisphosphatase deficiency - FDPase) impairs the body's ability to metabolize fructose from the diet.
  • Glomerulopathy with fibronectin deposits: An inherited form of kidney disease.
  • Glycogen Storage Disease Type I: An inherited metabolic disorder where a deficiency of the enzyme glucose-6-phosphatase prevents glycogen being turned into glucose leading to a buildup of glycogen in the liver and kidneys. Most problems tend to develop during adulthood.
  • Glycogen storage disease type 1C: A genetic metabolic disorder involving a deficiency of the enzyme glucose-6-phosphatase (due to a defect in the microsomal phosphate) which results in the accumulation of glycogen in various tissues. G6P is stored as glycogen until the body needs to convert it to a sugar for energy. The enzyme deficiency prevents the conversion and hence low blood sugar levels result.
  • Glycogen storage disease type 1D: A genetic metabolic disorder involving a deficiency of the enzyme glucose-6-phosphatase (due to a defect in the microsomal glucose transporter) which results in the accumulation of glycogen in various tissues. G6P is stored as glycogen until the body needs to convert it to a sugar for energy. The enzyme deficiency prevents the conversion and hence low blood sugar levels result.
  • Glycogen storage disease type 6: A rare, generally mild form of inherited glycogen storage disease where a deficiency of phosphorylase b kinase leads to hypoglycemia and accumulation of glycogen in the liver.
  • Glycogen storage disease type 6A, due to phosphorylase kinase deficiency: A rare, generally mild form of inherited glycogen storage disease where a deficiency of phosphorylase kinase leads to hypoglycemia and accumulation of glycogen in the liver. Phosphorylase kinase deficiency can cause glycogen storage disease type VIa and/or IX.
  • Glycogen storage diseases: A condition which is characterized by a defect in the ability of the body to store glycogen
  • Head symptoms: Symptoms affecting the head or brain
  • Herbal Agent overdose -- Germanium: Germanium is used as a health food supplement mainly in Japan but it can cause various problems if too much is taken. Chronic use and the ingestion of a large amount at one time can result in overdose symptoms.
  • Hereditary primary Fanconi disease: A rare inherited disorder characterized by defective reabsorption of various substances such as phosphate, potassium, amino acids and glucose which manifests as a wide range of abnormalities and problems.
  • Hydroxyacyl-coa dehydrogenase, type 2, deficiency: A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Some cases simply involve developmental delay.
  • Hyperemesis Gravidarum: An extreme form of morning sickness.
  • Hyperkalemic Renal Tubular Acidosis: A condition characterized by the inability of the kidneys to excrete acidic urine as well as an accumulation of potassium in the body
  • Hypoxia: This is where there is a reduction of oxygen supply to parts of the body below what is required for adequate perfusion
  • Inborn urea cycle disorder: A genetic disorder involving a deficiency of one of the enzymes needed in the urea cycle. The urea cycle is the process of removing ammonia from blood stream by converting it to urea and excreting it via urine. A build-up of ammonia in the blood is toxic to the body and can cause serious brain damage. The progressively severe symptoms usually become obvious within the first few weeks of birth. Nevertheless, mild or partial enzyme deficiencies may cause little or no symptoms or symptoms that don't start until later in life.
  • Infection: Infections as a symptom.
  • 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.
  • Ketoacidosis: A condition which is characterized by acidosis and the accumulation of ketone bodies in the body
  • Ketosis: The accumulation of ketone bodies in the body
  • Kidney conditions: Any condition affecting the kidney organs.
  • Lactic Acidosis: A condition which is characterized by the occurance of a metabolic acidosis due to the accumulation of lactic acid
  • Lactic acidosis: A condition which is characterized by the occurance of a metabolic acidosis due to the accumulation of lactic acid
  • Leukemia: Cancer of the blood cells, usually white blood cells.
  • Lipoamide dehydrogenase deficiency: A very rare enzyme deficiency (dihydrolipoamide dehydrogenase) which can cause lactic acidosis. The age of onset and symptoms are variable.
  • Lowe oculocerebrorenal syndrome: A rare inherited metabolic disorder characterized primarily by eye and bone abnormalities, mental retardation and kidney problems.
  • Lung conditions: Various conditions affecting the lungs or related airways.
  • Lung damage: When there is any damage to the structure or function of the lung
  • Lung symptoms: Symptoms affecting one or both lungs.
  • MELAS: A mitochondrial disorder characterized by stroke-like episodes, headaches, vomiting and other neurological symptoms.
  • MGA 4: MGA (methylglutaconic aciduria) is a rare genetic disorder where the body's cells are unable to make sufficient energy resulting in an accumulation in the body of 3-methylglutaconic acid. Type 4 is characterized by symptoms which overlap type 1 and 3.
  • Marasmus: A form of malnutrition caused by a severe deficiency of both protein and calories
  • Medium and long chan 3-hydroxyacyl-coenzyme A dehydrogenase deficiency: A metabolic disorder characterized by the deficiency of an enzyme (3-hydroxyacyl-coenzyme A dehydrogenase) which is needed to metabolise long and medum-chain fatty acids. The severity of symptoms may vary depending on the degree of the deficiency.
  • Metabolic disorder: occurs when abnormal chemical reactions occur in the body
  • Microvillus Inclusion Disease: A rare, inherited, progressive intestinal disease where a defect in the intestinal wall results in severe diarrhea after birth.
  • Mitochondrial DNA depletion syndrome: A group of conditions called mitochondrial disorders involving a reduced number of mitochondrial DNA in tissues rather than defective mitochondrial DNA. The disorders generally involve neurological symptoms which can occur during infancy or childhood. Symptoms will vary depending on the specific order involved.
  • Mitochondrial encephalomyopathy -- aminoacidopathy: A very rare syndrome characterized mainly by muscle and brain disease and an amino acid disorder.
  • Mitochondrial myopathy -- lactic acidosis: A very rare syndrome characterized mainly by muscle disease and a metabolic disorder. The severity and progression of the disease is variable with some dying early in their second decade and others living longer.
  • Mitochondrial neurogastrointestinal encephalopathy syndrome: A rare genetic disorder which affects a number of body systems and manifests results in symptoms such as droopy eyelids, progressive eye muscle weakness, gastrointestinal dysmotility, brain disease, thin body, peripheral neuropathy and muscle disease.
  • Multiple carboxylase deficiency, propionic acidemia: A disorder of fat metabolism where the body is unable to convert fat to energy due to the lack of a number of enzymes (carboxylases). Sufferers need to eat regularly to prevent symptoms. Symptoms are determined by the size and exact location of the tumor.
  • Muscle symptoms: Symptoms affecting the muscles of the body
  • Myopathy with lactic acidosis and sideroblastic anemia: A rare disorder of the bone marrow and skeletal muscles which manifests as muscle disease and anemia. Progressive intolerance to exercise usually starts during childhood with anemia occurring around adolescence.
  • NADH CoQ reductase, deficiency of: A rare genetic defect where an enzyme deficiency (NADH CoQ) disrupts cellular processes and causes various organic acid disorders. Any of a variety of the components of the enzyme may be missing or defective and hence the clinical presentation and severity may vary. Presentation may range from infantile death to various disorders neurodegenerative disorders such as Leigh's disease, Parkinson's disease and cardiomyopathy.
  • Necrotizing enterocolitis: A rare disease that is tends to occur in premature infants and involves inflammation and destruction of gastrointestinal tissue. It usually occurs within weeks of birth - often after the start of milk feeding. The condition can be extremely serious and even fatal.
  • 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
  • Neuromuscular disorder: neuromuscular disorders affect the nerves that control the voluntary muscles
  • Ondine syndrome: A rare condition involving defects in the mechanism that control breathing.
  • Ondine's curse: A condition involving defects in the mechanism that control breathing.
  • Organic acidemia: High blood levels of organic acids which is caused by abnormal protein metabolism. Maple syrup urine disease and propionic academia are examples of organic acidemias. Deficiency of certain metabolic enzymes one of the main causes of organic academia.
  • Osteopetrosis -- renal tubular acidosis: A rare disorder where increased bone density is caused by carbonic anhydrase II deficiency.
  • Osteopetrosis with renal tubular acidosis: A rare disorder where increased bone density is caused by carbonic anhydrase II deficiency.
  • Polyneuropathy -- Ophthalmoplegia -- Leukoencehalopathy -- Intestinal Pseudo-Obstruction: A rare genetic disorder which affects a number of body systems and manifests results in symptoms such as droopy eyelids, progressive eye muscle weakness, gastrointestinal dysmotility, brain disease, thin body, peripheral neuropathy and muscle disease.
  • Posthemorrhagic anemia: Posthemorrhagic anemia refers to a reduced number of red blood cells in the body due to bleeding.
  • Propionic Acidemia: A condition which is characterized by the excess of propionic acid and glycine in the blood resulting in acidaemia
  • Proximal Renal Tubular Acidosis: This is a condition that is characterised by a metabolic acidosis state caused by impairment of a persons renal function
  • Pyruvate carboxylase deficiency:
  • Pyruvate carboxylase deficiency, Group B: A rare inherited disorder characterized by a deficiency of pyruvate carboxylase which leads to accumulation of lactic acid and other compounds which can have a toxic effect on the nervous system and body organs. Type B has severe, life-threatening symptoms that can be noticed soon after birth.
  • Pyruvate carboxylase deficiency, Group C: A rare inherited disorder characterized by a deficiency of pyruvate carboxylase which leads to accumulation of lactic acid and other compounds which can have a toxic effect on the nervous system and body organs. Type C is a mild form of the condition.
  • Pyruvate decarboxylase deficiency: A rare genetic disorder involving an enzyme (pyruvate decarboxylase) deficiency which results in symptoms such as failure to thrive, psychomotor retardation, small head, eye problems, increased blood ammonia levels and lactic acidosis which can result in infant death in severe cases.
  • Pyruvate dehydrogenase phosphatase deficiency: A genetic disease involving an enzyme deficiency which causes exercise intolerance and mild developmental delay. Symptoms are variable.
  • Renal Tubular Acidosis: A rare disorder where the kidneys secrete too much hydrogen and don't reabsorb enough bicarbonate which can result in symptoms such as excessive blood acidity and loss of potassium.
  • Renal failure: A condition characterized by a failure of the kidney to excrete toxic metabolites from the body
  • SCHAD deficiency: A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Symptoms tend to be more severe in males who suffer progressive neurodegeneration whereas females tend to suffer mainly from developmental delay.
  • Shock: Physical and mental reaction to reduced circulation
  • Sjogren's Syndrome: Autoimmune disease damaging the eye tear ducts and other glands.
  • Succinic acidemia: A rare metabolic disorder characterized by high levels of succinic acid in the blood.
  • Succinic acidemia -- lactic acidosis, congenital: A very rare disorder characterized by high levels of succinic acid in the blood and high blood acidity which starts at birth or soon after.
  • Swollen bone: Enlarged, swollen, or misshapen bones
  • Thinness: Underweight and thin
  • Tiglic acidemia: Increased blood tiglic acid levels due to a metabolic disorder involving the breakdown of isoleucine to propionic acid.
  • Tissue hypoxia: inadequate blood supply to a a particular body part
  • Toni-Fanconi syndrome type 1:
  • Type 10 17b-hydroxysteroid dehydrogenase deficiency: A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Symptoms tend to be more severe in males who suffer progressive neurodegeneration whereas females tend to suffer mainly from developmental delay.
  • Type I Glycogen Storage Disease: A condition which is characterized by a disease affecting glycogen storage
  • Von Gierke Disease: An inherited metabolic disorder where a deficiency of the enzyme glucose-6-phosphatase prevents glycogen being turned into glucose leading to a buildup of glycogen in the liver and kidneys.
  • Wilson's disease: Wilson disease, or hepatolenticular degeneration, is a neurodegenerative disease of copper metabolism.

Conditions listing medical symptoms: Acidosis:

The following list of conditions have 'Acidosis' 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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Conditions listing medical complications: Acidosis:

The following list of medical conditions have 'Acidosis' or similar listed as a medical complication in our database.

 

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