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Breath sound symptoms and Electrolyte imbalance and Barrett's oesophagus-like weight loss symptoms and Emotional symptoms
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Breath sound symptoms and Electrolyte imbalance and Barrett's oesophagus-like weight loss symptoms and Emotional symptoms

  • Breath sound symptoms AND Electrolyte imbalance AND Barrett's oesophagus-like weight loss symptoms AND Emotional symptoms - Causes of All Symptoms
  • Breath sound symptoms OR Electrolyte imbalance OR Barrett's oesophagus-like weight loss symptoms OR Emotional symptoms - 2674 causes

Breath sound symptoms:

Electrolyte imbalance:

Barrett's oesophagus-like weight loss symptoms:

Emotional symptoms:

Results: Causes of Breath sound symptoms AND Electrolyte imbalance AND Barrett's oesophagus-like weight loss symptoms AND Emotional symptoms

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

Results: 2674 causes of Breath sound symptoms OR Electrolyte imbalance OR Barrett's oesophagus-like weight loss symptoms OR Emotional symptoms

    1. 14q+ syndrome
     A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....more »
    2. 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 »
    3. 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 »
    4. 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 »
    5. 22q11.2 deletion syndrome
     A rare genetic disorder caused by the absence of a small portion of genetic material. A small section of chromosome 22 is missing at a location called q11.2. Chromosome 22 is one of 23 pairs of chromosomes that exist in humans....more »
    6. 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency
     A very rare metabolic disorder where a deficiency of a particular enzyme results in the urinary excretion of a chemical called hawkinsin. Symptoms start once the infant is weaned off breast milk....more »
    7. 47,XXX syndrome
     A genetic condition where females have an extra X chromosome in each of their cells. Normally female cells have two X chromosomes. This is not usually an inherited condition but a defect that occurs during cell division. Often the condition is asymptomati...more »
    8. 49,XXXXY syndrome
     A rare sex chromosome abnormality where there are three extra copies of the X chromosome....more »
    9. Aberrant subclavian artery abnormality
     A rare defect where one the subclavian artery arises from an abnormal location on the aortic arch. The defect may cause compression of organs such as the airway and the voice box....more »
    10. Acanthamoeba infection
     Infection with a microscopic, free-living ameba that is readily found in the environment - soil, air and water. Most people exposed to the ameba will not become infected but when infections do occur, they tend to affect the eyes, central nervous system or...more »

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  • Warning - Beta version - information may be incorrect (details)
  • Disclaimer - Do not use this information for diagnosis (details)
  • Important - See your doctor - Only a doctor can give an accurate diagnosis (details)
 

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