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Altered bowel habit in pregnancy and Coma and Heavy periods and Sensory symptoms
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Altered bowel habit in pregnancy and Coma and Heavy periods and Sensory symptoms

  • Altered bowel habit in pregnancy AND Coma AND Heavy periods AND Sensory symptoms - Causes of All Symptoms
  • Altered bowel habit in pregnancy OR Coma OR Heavy periods OR Sensory symptoms - 7242 causes

Altered bowel habit in pregnancy:

Coma:

Heavy periods:

Sensory symptoms:

Results: Causes of Altered bowel habit in pregnancy AND Coma AND Heavy periods AND Sensory symptoms

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

Results: 7242 causes of Altered bowel habit in pregnancy OR Coma OR Heavy periods OR Sensory symptoms

    1. 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 »
    2. 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 »
    3. 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency
     A rare inherited disorder where lack of a certain enzyme (3-methylcrotonyl-Coa carboxylase) stops proteins with the amino acid leucine being metabolized normally by the body. The leucine builds up in the body and causes damage to the brain and nervous sys...more »
    4. 3 alpha methylcrotonyl-coa carboxylase 2 deficiency
     A rare inherited disorder where lack of a certain enzyme (3-methylcrotonyl-Coa carboxylase) stops proteins with the amino acid leucine being metabolized normally by the body. The leucine builds up in the body and causes damage to the brain and nervous sys...more »
    5. 3-alpha-Hydroxyacyl-CoA Dehydrogenase Deficiency
     A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activit...more »
    6. 3-alpha-hydroxyacyl-coenzyme A dehydrogenase deficiency
     A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activit...more »
    7. 3-methylcrotonyl-CoA carboxylase deficiency
     A rare inherited disorder where lack of a certain enzyme (3-methylcrotonyl-Coa carboxylase) stops proteins with the amino acid leucine being metabolized normally by the body. The leucine builds up in the body and causes damage to the brain and nervous sys...more »
    8. AAA
     Anoutpouching at an area of weakness in the abdominal aorta involving all 3 layers of the artery wall....more »
    9. Abalone poisoning
     Abalone are a shellfish that are commonly eaten by humans. The internal organs of the abalone sometimes contain toxins which can cause various symptoms. The toxins are believed to originate from toxic components in the abalones diet....more »
    10. Abdominal abscess
     An abscess that occurs anywhere in the abdomen....more »

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Notes About Causes

  • 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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