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Symptom Checker » Abnormal heart rhythm » Acute kidney failure
 

Abnormal heart rhythm and Acute kidney failure and Nausea and Skin symptoms
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Abnormal heart rhythm and Acute kidney failure and Nausea and Skin symptoms

  • Abnormal heart rhythm AND Acute kidney failure AND Nausea AND Skin symptoms - Causes of All Symptoms
  • Abnormal heart rhythm OR Acute kidney failure OR Nausea OR Skin symptoms - 6986 causes

Abnormal heart rhythm:

Acute kidney failure:

Nausea:

Skin symptoms:

Results: Causes of Abnormal heart rhythm AND Acute kidney failure AND Nausea AND Skin symptoms

    1. Chemical poisoning -- Phosphine
     Phosphine is a chemical used mainly in pesticides and rodenticides. 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 expos...read more »

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Note: Do not use for diagnosis; see limitations of results.

Results: 6986 causes of Abnormal heart rhythm OR Acute kidney failure OR Nausea OR Skin symptoms

    1. 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 »
    2. 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 »
    3. 2q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    4. 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....more »
    5. 3?-hydroxysteroid dehydrogenase deficiency
     A ver rare form of congenital adrenal hyperplasia involving a deficiency of 3?-hydroxysteroid dehydrogenase which results in reduced production of adrenal steroids (mineralocorticoids, sex steroids and glucocorticoids). The disorder can occur in classical...more »
    6. 3C syndrome
     A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name....more »
    7. 46,XX Gonadal dysgenesis epibulbar dermoid
     A rare disorder characterized by gonad abnormalities and an eye disorder called epibulbar dermoid....more »
    8. 4p16.3 deletion
     A rare genetic disorder where a portion of chromosome 4 is deleted at a location called 16.3. The condition is characterized by malformations in most parts of the body as the deletion affects growth and development of the fetus....more »
    9. Aantibodies anti-FVIIIc syndrome
     A rare, acquired blood condition where the body develops antibodies against a blood clotting factor (FVIII) which results in bleeding problems....more »
    10. Aarskog Syndrome
     A rare genetic condition characterized by facial, hand, genital and growth abnormalities....more »

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  • Warning - Beta version - information may be incorrect (details)
  • Disclaimer - Do not use this information for diagnosis (details)
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