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Symptom Checker » Chest tightness » Difficulty concentrating at school
 

Chest tightness and Difficulty concentrating at school and Fatigue and Muscle weakness and Nausea and Palpitations during pregnancy
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Chest tightness and Difficulty concentrating at school and Fatigue and Muscle weakness and Nausea and Palpitations during pregnancy

  • Chest tightness AND Difficulty concentrating at school AND Fatigue AND Muscle weakness AND Nausea AND Palpitations during pregnancy - Causes of All Symptoms
  • Chest tightness OR Difficulty concentrating at school OR Fatigue OR Muscle weakness OR Nausea OR Palpitations during pregnancy - 5747 causes

Chest tightness:

Difficulty concentrating at school:

Fatigue:

Muscle weakness:

Nausea:

Palpitations during pregnancy:

Results: Causes of Chest tightness AND Difficulty concentrating at school AND Fatigue AND Muscle weakness AND Nausea AND Palpitations during pregnancy

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

Results: 5747 causes of Chest tightness OR Difficulty concentrating at school OR Fatigue OR Muscle weakness OR Nausea OR Palpitations during pregnancy

    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. 14q+ syndrome
     A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....more »
    3. 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 »
    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. 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 »
    7. 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 »
    8. 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 »
    9. 2p21 deletion syndrome
     This syndrome is a more severe form hypotonia-cystinuria syndrome as a larger portion of genetic material from chromosome 2p21 is deleted. It is characterized by infant seizures, reduced muscle tone, developmental delay, lactic acidosis and unusual facial...more »
    10. 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 »

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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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