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Symptom Checker » Joints inflammation » Puffy eyes
 

Joints inflammation and Puffy eyes and Eating symptoms and Stomach symptoms
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Joints inflammation and Puffy eyes and Eating symptoms and Stomach symptoms

  • Joints inflammation AND Puffy eyes AND Eating symptoms AND Stomach symptoms - Causes of All Symptoms
  • Joints inflammation OR Puffy eyes OR Eating symptoms OR Stomach symptoms - 4422 causes

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Results: Causes of Joints inflammation AND Puffy eyes AND Eating symptoms AND Stomach symptoms

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

Results: 4422 causes of Joints inflammation OR Puffy eyes OR Eating symptoms OR Stomach 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. 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 »
    4. 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 »
    5. 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 »
    6. 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 »
    7. 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 »
    8. 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 »
    9. 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 »
    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)
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