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Symptom Checker » Abdominal symptoms » Acute disorientation
 

Abdominal symptoms and Acute disorientation and Buttock numbness and Coma in children and Disorientation
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Abdominal symptoms and Acute disorientation and Buttock numbness and Coma in children and Disorientation

  • Abdominal symptoms AND Acute disorientation AND Buttock numbness AND Coma in children AND Disorientation - Causes of All Symptoms
  • Abdominal symptoms OR Acute disorientation OR Buttock numbness OR Coma in children OR Disorientation - 5867 causes

Abdominal symptoms:

Acute disorientation:

Buttock numbness:

Coma in children:

Disorientation:

Results: Causes of Abdominal symptoms AND Acute disorientation AND Buttock numbness AND Coma in children AND Disorientation

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

Results: 5867 causes of Abdominal symptoms OR Acute disorientation OR Buttock numbness OR Coma in children OR Disorientation

    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. 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 »
    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. 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 »
    7. 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 »
    8. 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 »
    9. 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 »
    10. 46,XX testicular disorder of sex development
     A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY....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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