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Symptoms » Cardiomyopathy » Glossary
 

Glossary for Cardiomyopathy

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

  • 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.
  • African Sleeping sickness: A disease caused by parasites (Trypanosome brucei gamiense or T. brucei rodesiense) and transmitted to humans by the tsetse fly which is found only in Africa. Causes symptoms such as fever, chills, headache, anemia, edema of hands and feet, enlarged lymph glands, lethargy, sleepiness, convulsions and coma. Also called African trypanosomiasis and sleeping sickness.
  • Alcohol abuse: Excessive alcohol as a symptom of other conditions
  • Alcoholism: High dependence on excessive amounts of alcohol.
  • Alpers Syndrome: A rare syndrome characterized by liver disease, seizures and progressive, episodic psychomotor retardation.
  • Amyloidosis: A disease characterized by the accumulation of insoluble amyloid protein in tissues and organs which in turn affects the functioning of these tissues and organs.
  • Arrhythmogenic right ventricular dysplasia: A rare heart muscle disease where the muscle tissue of the right ventricle of the heart is replaced by fibrous or fatty tissue which affects the ability of the heart to pump blood.
  • Arterial calcification of infancy: A rare disorder involving widespread calcification of arteries which obstructs blood flow.
  • Arthritis -- short stature -- deafness: A very rare syndrome characterized by arthritis, short stature, deafness and numerous other abnormalities.
  • Arthrogryposis due to muscular dystrophy: A rare disorder where a non-progressive muscle disease results in the presence of multiple joint contractures at birth.
  • Barth Syndrome: 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 2 is characterized by its affects on the heart.
  • Borud Syndrome: A very rare syndrome characterized by numerous features including hearing and vision problems, heart muscle disease, ataxia and peripheral neuropathy.
  • Breathing difficulties: Various types of breathing difficulty (dyspnea).
  • CDG syndrome type 1A: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1A involves a phosphomannomutase enzyme defect and affects most body systems especially the nervous system and liver function.
  • Carcinoid syndrome: Carcinoid heart disease is a rare, metastatic disease that occurs predominantly in the right heart. The tricuspid and pulmonic valves are affected, leading to right heart failure, which results in increased morbidity and mortality.
  • Cardiomyopathy -- hearing loss, type tRNA-LYS gene mutation: A rare inherited condition characterized by the association of cardiomyopathy and deafness.
  • Cardiomyopathy -- hypogonadism -- metabolic anomalies: A rare syndrome characterized mainly by heart muscle disease, hypogonadism, blindness, deafness and metabolic anomalies. Puberty was normal despite the hypogonadism.
  • Cardiomyopathy -- renal anomalies: A rare syndrome characterized by heart muscle disease and defects in the genitourinary system.
  • Cardiomyopathy -- spherocytosis: A rare disorder characterized by the association of spherocytosis with heart muscle disease. Spherocytosis is a red blood cell disorder where the red blood cells have abnormal membranes which gives them a spherical shape and makes them weak resulting in their premature death.
  • Cardiomyopathy diabetes deafness: A rare syndrome characterized by the association of heart muscle disease, diabetes and deafness.
  • Cardiomyopathy due to anthracyclines: Damage to the heart muscle caused by anthracycline drugs which are used in chemotherapy. The damage occurs more frequently with higher cumulative doses. Often the patients have no symptoms of the heart damage for many year.
  • Cardiomyopathy with myopathy due to COX deficency: A rare condition where an enzyme (cytochrome c oxidase) deficiency results in muscle disease which also affects the heart.
  • Cardiomyopathy, X-linked, fatal infantile: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The condition occurs during infancy and results in death.
  • Cardiotoxicity -- Adrenergic beta-receptor agonists: Exposure to many adrenergic beta-receptor agonists can have a toxic effect on the heart and may result in cardiomyopathy. The degree of toxicity may be influenced the duration and level of exposure to the chemical.
  • Cardiotoxicity -- Allylamine: Exposure to Allylamines can have a toxic effect on the heart and may result in degenerative changes in the heart. The degree of toxicity may be influenced the duration and level of exposure to the chemical.
  • Cardiotoxicity -- Certain Antihypertensive Drugs: Exposure to certain antihypertensive drugs can have a toxic effect on the heart and may result in cardiomyopathy. The degree of toxicity may be influenced the duration and level of exposure to the chemical.
  • Cardiotoxicity -- Cobalt: Exposure to Cobalt can have a toxic effect on the heart and may result in cardiomyopathy. The degree of toxicity may be influenced the duration and level of exposure to the chemical.
  • Cardiotoxicity -- Ethanol: Exposure to Cobalt can have a toxic effect on the heart and may result in cardiomyopathy. The degree of toxicity may be influenced the duration and level of exposure to the chemical.
  • Cardiotoxicity -- Hydralazine: Exposure to Hydralazine (an antihypertensive drug) can have a toxic effect on the heart and may result in cardiomyopathy. The degree of toxicity may be influenced the duration and level of exposure to the chemical.
  • Cardiotoxicity -- Streptomycin: Exposure to Streptomycin can have a toxic effect on the heart and may result in cardiomyopathy. The degree of toxicity may be influenced the duration and level of exposure to the chemical.
  • Cardiovascular symptoms: Symptoms affecting the heart and related vascular systems.
  • Carnitine palmitoyl transferase 2 deficiency: A very rare inherited deficiency of a particular enzyme (Carnitine palmitoyl transferase) which prevents fatty acids being transported to the part of the cell that converts it to energy. There are two main subtypes of the disorder with each involving a slightly different form of the enzyme. Type I can be readily managed through diet. Type II has three subtypes: the myopathic form affects mainly the muscles; the hepatocardiomuscular form affects the liver and heart muscle; and the lethal neonatal form affects muscles and organs and usually results in death during the first year of life.
  • Carnitine transporter deficiency: An inherited deficiency of carnitine caused by the impaired ability of the carnitine transporter protein to carry the carnitine to where it is needed. Instead the carnitine is excreted through the urine. Fasting or illness can trigger a severe attack.
  • 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 -- Thallium: Thallium is an element used for such things as electronic devices, selenium rectifiers, gamma radiation detection apparatus, transmission equipment and infrared radiation detection. It is also used as a catalyst in various manufacturing processes. 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.
  • Chest pain: Any chest pain must be considered as cardiac in origin until proven otherwise.
  • Chromosome 1, 1p36 deletion syndrome: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as heart problems, mental retardation, developmental delay, facial dysmorphism and short stature. The symptoms are variable depending on the exact location of chromosomal deletion.
  • Chromosome 11, deletion 11p: A syndrome that is caused by the deletion of short arm (p) of chromosome 11. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is deleted.
  • Cobalt poisoning: A type of heavy metal poisoning caused by excessive exposure to cobalt.
  • Coenzyme Q 10 (CoQ10), deficiency: A rare inherited disorder characterized by the deficiency of Coenzyme Q 10. The range and severity of symptoms is variable.
  • 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.
  • Collagenoma, cutaneous familial: A rare inherited condition characterized primarily by skin nodules.
  • 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.
  • Complex 5 mitochondrial respiratory chain deficiency: A rare genetic defect where an enzyme deficiency (ATP synthetase) 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 Leber's myopathy, Leigh syndrome, cardiomyopathy and NARP (neuropathy, ataxia, retinitis pigmentosa).
  • Congenital Disorders of Glycosylation Type Ia: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1A involves a phosphomannomutase enzyme defect and affects most body systems especially the nervous system and liver function.
  • Congenital disorder of glycosylation type 1A: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1A involves a phosphomannomutase enzyme defect and affects most body systems especially the nervous system and liver function.
  • Congenital disorder of glycosylation type 1G: Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type IG is caused by a defect on chromosome 22q13.33 and involves the gene for a particular enzyme (dolichyl-P-mannose:Man-7-GlcNAc-2-PP-dolichyl-alpha-6-mannosyltransferase).
  • Congenital disorder of glycosylation type 1K: Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type Ik is caused by a defect on chromosome 16p13.3 and involves a defect in the gene for beta-1,4-mannosyltransferase. The disorder is generally fatal within a year or two of birth.
  • Congenital disorder of glycosylation type 1M: Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type Im is caused by a defect on chromosome 9q34.11 and involves a defect in the TMEM15 gene.
  • Congenital heart disease: Diseases of the heart that one is born with
  • Cytochrome C Oxidase Deficiency: Cytochrome C oxidase deficiency is a rare inherited condition involving insufficient quantities of the cytochromc C oxidase enzyme. This enzyme plays a role in the functioning of the energy producing part of body cells (mitochondria) and its deficiency impairs the energy-producing functions of the cells. The type and severity of symptoms can vary considerably depending on which particular cells in the body are affected and the degree of the enzyme deficiency. In some cases only skeletal muscles are affected whereas in other cases organs such as the heart and brain are involved. In other cases, the whole body may be involved.
  • Del(1) (pter-p36.2): A very rare chromosomal disorder where the end portion of the short arm of chromosome one is missing. The type and severity of symptoms is variable.
  • Deletion 11p: A syndrome that is caused by the deletion of short arm (p) of chromosome 11. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is deleted.
  • Diabetes insipidus, diabetes mellitus, optic atrophy: A rare association of diabetes insipidus, diabetes mellitus, optic atrophy, and deafness.
  • Diabetes-like symptoms: Symptoms similar to those of diabetes
  • Doxorubicin -- Teratogenic Agent: There is evidence to indicate that exposure to Doxorubicin (a chemotherapy 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.
  • Duchenne Muscular Dystrophy: An inherited degenerative disease of the muscles which progresses rapidly compared to other muscle wasting diseases.
  • Emery-Dreifuss Muscular Dystrophy 2: A rare inherited condition characterized mainly by slowly progressive muscle wasting which tends to start during childhood as well as joint contractures and heart conduction defects. Type 2 is linked to a defect on chromosome 1q21.2. Because the condition is inherited in an autosomal dominant manner so males and females may be affected.
  • Emery-Dreifuss muscular dystrophy, X-linked: A muscle wasting disorder mainly involving the muscles in the arms, legs, face, neck, spine and heart. Symptoms generally only occur in males but female carriers may have some symptoms.
  • Ethanol -- Teratogenic Agent: There is evidence to indicate that exposure to Ethanol 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.
  • Facio-cardio-musculo-skeletal syndrome: A rare syndrome characterized by facial, heart, muscle and skeletal abnormalities.
  • Fenfluramine -- Teratogenic Agent: There is evidence to indicate that exposure to Fenfluramine (a weight loss 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.
  • HIV/AIDS: HIV is a sexually transmitted virus and AIDS is the progressive immune failure that HIV causes.
  • HOCM: Hypertrophic obstructive cardiomyopathy
  • Head symptoms: Symptoms affecting the head or brain
  • Heart disease: Any disease that affects that heart but particularly relating to its own blood supply
  • Heart failure: A condition which is characterized by an inability of the heart to pump blood efficiently and effectively
  • Heart symptoms: Symptoms affecting the heart
  • Heart valve disorder:
  • Hemochromatosis: Excess of iron leading to problems with joints, liver, heart and pancreas.
  • Hereditary carnitine deficiency: An inherited deficiency of carnitine resulting primarily in muscle problems. Severe symptoms can be triggered by periods of illness or fasting.
  • Hereditary carnitine deficiency myopathy: An inherited deficiency of carnitine resulting primarily in muscle weakness.
  • Hereditary carnitine deficiency syndrome: An inherited deficiency of carnitine resulting primarily in muscle weakness. The carnitine deficiency may be due to excessive loss of insufficient production.
  • Hereditary carnitine deficiency syndrome, myopathic: An inherited deficiency of carnitine in muscles resulting primarily in muscle weakness - generally less severe than the systemic form.
  • Hereditary carnitine deficiency syndrome, systemic: An inherited deficiency of carnitine in tissues other than the muscles resulting primarily in muscle weakness.
  • High Blood Iron: Where a patient has an elevated iron content of their blood
  • High blood pressure: Excessive blood pressure.
  • Human carcinogen -- Cyclophosphamide: Cyclophosphamide is a chemical deemed to be carcinogenic to humans. The carcinogenicity of the substance may be influenced by the nature (e.g. inhalation, ingestion, skin contact), duration and level of exposure. Cyclophosphamide exposure is associated mainly with an increased risk of developing leukemia.
  • Hutchinson Gilford Syndrome: A rare genetic disorder characterized by alopecia and senile-like appearance.
  • Hypereosinophilic syndrome: A rare condition where too many eosinophils are produced over an extended period of time for no apparent reason. The eosinophils can infiltrate various organs and tissues and cause dysfunction or damage
  • Hyperthyroidism: The excessive activity of the thyroid gland
  • Immunoglobulinic amyloidosis: A disease characterized by the abnormal deposit of amyloid in various parts of the body, especially organs such as the kidneys, heart, liver, gastrointestinal tract and peripheral nerves. It occurs when plasma cells in the bone marrow produce too much of a protein portion of an antibody called the light chain. The exact symptoms are determined by the extent of the organ involvement.
  • Ischemic heart disease: Heart disease from reduced blood flow to the heart
  • Kearns-Sayre Syndrome: A rare neuromuscular disorder characterized by pigmented deposits on the retina, heart disease and progressive paralysis of some eye muscles.
  • Keshan disease: A heart muscle disease believed to be caused by a deficiency of the mineral called selenium in the diet.
  • Limb-girdle Muscular Dystrophy: A condition which is characterized by a slowly progressive muscular dystrophy
  • Limb-girdle muscular dystrophy type 2C: An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of the gamma-sarcoglycan gene. The severity of the condition is greatly variable from wheelchair confinement at the age of 9 years to asymptomatic adults. Most tend to live to their third decade.
  • Limb-girdle muscular dystrophy type 2D: An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of the alpha-sarcoglycan gene. The severity of the condition is greatly variable from wheelchair confinement at the age of 9 years to asymptomatic adults. Most tend to live to their third decade.
  • Limb-girdle muscular dystrophy type 2E: An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of the beta-sarcoglycan gene. The severity of the condition is greatly variable from wheelchair confinement at the age of 9 years to asymptomatic adults. Most tend to live to their third decade.
  • Limb-girdle muscular dystrophy type 2F: An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of the delta-sarcoglycan gene. The severity of the condition is greatly variable from wheelchair confinement at the age of 9 years to asymptomatic adults. Most tend to live to their third decade.
  • Limb-girdle muscular dystrophy type 2I: An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of the FKRP (fukutin-related protein) gene.
  • 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.
  • Malonic aciduria: A very rare genetic disorder where a deficiency of a particular enzyme (malonyl-CoA decarboxylase) impairs the body's ability to convert fatty acids into energy that can be used by muscles such as the heart muscle. Fatty acids also accumulate in the body as they are not metabolized.
  • Metaphyseal chondrodysplasia, recessive type: A recessively inherited skeletal disorder characterized by abnormal development of the bone metaphyses which results in short stature from birth.
  • Microphthalmia, syndromic 7: A rare genetic disorder characterized by eye and skin abnormalities involving irregular red streaks of skin on the head and neck.
  • Mitochondrial trifunctional protein deficiency: A rare genetic condition where the body is unable to convert certain fats to energy. More specifically, there is insufficient levels of a particular enzyme needed to metabolize a type of fat called long-chain fatty acids.
  • Movement symptoms: Changes to movement or motor abilities
  • Mucopolysaccharidosis type I Hurler syndrome: A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of the enzyme (?-L-diuronidase) needed to break it down. There are three main sub-types of the disorder: Hurler - severe form, Scheie - mild form and Hurler/Scheie form which is intermediate.
  • Muscle symptoms: Symptoms affecting the muscles of the body
  • Muscle weakness: Weakness of the muscles or loss of tone
  • Muscular dystrophy, limb-girdle, autosomal recessive, type 2E: An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of the beta-sarcoglycan gene. The severity of the condition is greatly variable from wheelchair confinement at the age of 9 years to asymptomatic adults. Most tend to live to their third decade.
  • Musculoskeletal symptoms: Symptoms affecting muscles or bones of the skeleton.
  • Myocarditis: A condition which is characterized by inflammation of the muscles of the heart
  • Myopathy: Any disease that occurs in the muscle.
  • Myotonic Dystrophy: An inherited disorder characterized by progressive muscle weakness and wasting as well as eye defects, heart abnormalities and other anomalies. The severity of the condition is greatly variable. There are two type of myotonic dystrophy with type 1 being more severe than type 2.
  • 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.
  • Nerve symptoms: Symptoms affecting the nerves
  • Obesity -- colitis -- hypothyroidism -- cardiac hypertrophy -- developmental delay: A rare syndrome characterized by obesity, colitis, hypothyroidism, enlarged heart and developmental delay. The two reported cases involved maternal HELLP syndrome during pregnancy. Both infants died within months of birth.
  • Paracetamol -- Teratogenic Agent: There is evidence to indicate that exposure to Paracetamol 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.
  • Pheochromocytoma: pheochromocytoma is a rare tumor that usually starts in the cells of the adrenal glands
  • Possible human carcinogenic exposure -- Bleomycin: Some evidence indicates that exposure to Bleomycin has a possible link to an increased risk of developing cancer in humans. The carcinogenicity of the substance may be influenced by the duration and level of exposure. Bleomycin is used primarily as a chemotherapy drug.
  • Possible human carcinogenic exposure -- Lead: Some evidence indicates that exposure to Lead has a possible link to an increased risk of developing cancer in humans. The carcinogenicity of the substance may be influenced by the duration and level of exposure.
  • Possible human carcinogenic exposure -- Mitoxantrone: Some evidence indicates that exposure to Mitoxantrone (a chemotherapy drug) has a possible link to an increased risk of developing cancer in humans. The carcinogenicity of the substance may be influenced by the duration and level of exposure.
  • Potassium deficiency: A deficiency of potassium in the body
  • Refsum Disease: A metabolic disorder where a deficiency of phytanic acid alpha-hydroxylase results in a buildup of phytanic acid in the body which causes neurological disorders.
  • Refsum disease with increased pipecolic acidemia: A rare disorder involving all the clinical features of Refsum disease as well as high blood levels of L-pipecolic acid. Refsum disease is a metabolic disorder where a deficiency of phytanic acid alpha-hydroxylase results in a buildup of phytanic acid in the body which causes neurological disorders.
  • Restrictive cardiomyopathy: A condition which is characterized by restriction to the function of the walls of the heart
  • Sarcoglycanopathy: A form of limb-girdle muscular dystrophy involving abnormalities of the sarcoglycan protein which results in progressive muscle weakness. The severity is greatly variably from wheelchair confinement at the age of 9 years to asymptomatic adults. Most tend to live to their third decade.
  • Scapuloperoneal myopathy: An inherited disorder involving muscle wasting and weakness in the shoulder and lower leg.
  • Scleroderma: A rare, progressive connective tissue disorder involving thickening and hardening of the skin and connective tissue. There are a number of forms of scleroderma with some forms being systemic (involving internal organs).
  • Shortness of breath: The feeling of being short of breath
  • Sonoda syndrome: An extremely rare disorder characterized by a congenital heart defect, round face, retarded development, short stature and various facial anomalies.
  • Tacrolimus -- Teratogenic Agent: There is evidence to indicate that exposure to Tacrolimus 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.
  • Thiamine deficiency: Dietary deficiency of vitamin B1 (thiamine)
  • Toxic mushrooms -- cyclopeptides: Some mushrooms contain a toxic chemical called cyclopeptide which can cause primarily gastrointestinal symptoms if ingested. Most cases of mushroom poisoning in North America involve cyclopeptide-containing mushrooms. Mushroom species from this group include certain species of Amanita (bisporigera, ocreata, phalloides, suballiacea, tenufolia, verna, virosa), Galerina and Lepiota. One Amanita mushroom cap may result in death in an adult. Poisoning occurs in three phases: gastrointestinal symptoms (within 24 hours of ingestion); remission (up to 72 hours after ingestion); and liver and kidney symptoms (3 to 6 days after ingestion). Poisoning symptoms are more severe in children due to their smaller body size.
  • Triose phosphate-isomerase deficiency: A very rare inherited condition involving a deficiency of triose phosphate-isomerase.
  • Viral diseases: Any disease that is caused by a virus
  • WAGR Syndrome: A syndrome that is due to the deletion of chromosome 11.
  • Wilms tumor -- aniridia -- genitourinary anomalies -- mental retardation: A syndrome resulting from deletion of genetic material from chromosome the short arm of chromosome 11 (11p13). The characteristic symptoms are partial or complete absence of iris, genitourinary anomalies, mental retardation and Wilms' tumor. The specific range and severity of symptoms is variable depending on the size and exact location of the genetic material that is missing.
  • 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: Cardiomyopathy:

The following list of conditions have 'Cardiomyopathy' 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: Cardiomyopathy:

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

 

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