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Mania and Nerve symptoms and Sexual symptoms and Skin symptoms and Heart rhythm symptoms and Stool symptoms
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Mania and Nerve symptoms and Sexual symptoms and Skin symptoms and Heart rhythm symptoms and Stool symptoms

  • Mania AND Nerve symptoms AND Sexual symptoms AND Skin symptoms AND Heart rhythm symptoms AND Stool symptoms - Causes of All Symptoms
  • Mania OR Nerve symptoms OR Sexual symptoms OR Skin symptoms OR Heart rhythm symptoms OR Stool symptoms - 11894 causes

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Results: Causes of Mania AND Nerve symptoms AND Sexual symptoms AND Skin symptoms AND Heart rhythm symptoms AND Stool symptoms

    1. Cathinone poisoning
     Cathinone comes from the leaves of the Khat plant which is native to eastern Africa. Cathinone is a stimulant as well as have pain killing, weight loss and neuromuscular effects. The psychoactive effects are usually utilized by chewing on the leaves of th...read more »
    2. Chemical poisoning -- Azinphos-methyl
     Azinphos-methyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on ...read more »
    3. Hyperthyroidism -- Teratogenic Agent
     There is strong evidence to indicate that the development of hyperthyroidism 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 th...read more »
    4. Lymphomatous thyroiditis
     Progressive thyroid gland enlargement due to autoimmune disease....read more »

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Results: 11894 causes of Mania OR Nerve symptoms OR Sexual symptoms OR Skin symptoms OR Heart rhythm symptoms OR Stool symptoms

    1. 10q Partial Trisomy
     A very rare genetic disorder characterized by the duplication of genetic material from the long arm (q) of chromosome 10 - the genetic material occurs three times in body cells instead of the normal two. The type and severity of symptoms may vary consider...more »
    2. 14qter deletion Syndrome
     A very rare genetic condition where a portion at the end of the long arm (q) of chromosome 14 is missing....more »
    3. 17-Beta-hydroxysteroid dehydrogenase III deficiency
     A rare disorder characterized caused by an enzyme (17-ketosteroid reductase) defect only in the testes which results in a lack of testosterone which is needed during the fetal stage to give males there physical characteristics....more »
    4. 18p minus syndrome
     A rare chromosomal disorder where a portion of chromosome 18 is missing which is characterized by mental and growth deficiencies, drooping upper eyelid and prominent ears. The type and severity of symptoms is determined by the amount of genetic material t...more »
    5. 1q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    6. 1q terminal deletion
     A rare chromosomal disorder where the terminal part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities....more »
    7. 2-Hydroxyglutaricaciduria
     A rare metabolic disorder characterized by high levels of a certain chemical (2-Hydroxyglutaric) which causes a serious progressive neurological disease and damage to the brain. The features of this disorder are variable and some cases are milder than oth...more »
    8. 2-Methylbutyric Aciduria
     A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...more »
    9. 2-hydroxyethyl methacrylate sensitization
     A condition where exposure to 2-hydroxyethyl methacrylate results in sensitization to the chemical - further exposure to the chemical causes a reaction. The chemical is used in dental work so dental patients and dental workers are at risk of becoming sens...more »
    10. 2-methylbutyryl-coenzyme A dehydrogenase deficiency
     A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...more »

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