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Chronic diseases causing fatigue in children and Mania and Nerve symptoms and Skin symptoms and Heart rhythm symptoms and Stool symptoms
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Chronic diseases causing fatigue in children and Mania and Nerve symptoms and Skin symptoms and Heart rhythm symptoms and Stool symptoms

  • Chronic diseases causing fatigue in children AND Mania AND Nerve symptoms AND Skin symptoms AND Heart rhythm symptoms AND Stool symptoms - Causes of All Symptoms
  • Chronic diseases causing fatigue in children OR Mania OR Nerve symptoms OR Skin symptoms OR Heart rhythm symptoms OR Stool symptoms - 11521 causes

Chronic diseases causing fatigue in children:

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Results: Causes of Chronic diseases causing fatigue in children AND Mania AND Nerve symptoms AND Skin symptoms AND Heart rhythm symptoms AND Stool symptoms

    1. Hyperthyroidism -- Teratogenic Agent
     There is strong evidence to indicate that the development of hyperthyroidism during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by th...read more »

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Results: 11521 causes of Chronic diseases causing fatigue in children OR Mania OR Nerve symptoms OR Skin symptoms OR Heart rhythm symptoms OR Stool symptoms

    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. 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 »
    3. 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 »
    4. 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 »
    5. 1q terminal deletion
     A rare chromosomal disorder where the terminal part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities....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-hydroxyethyl methacrylate sensitization
     A condition where exposure to 2-hydroxyethyl methacrylate results in sensitization to the chemical - further exposure to the chemical causes a reaction. The chemical is used in dental work so dental patients and dental workers are at risk of becoming sens...more »
    9. 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 »
    10. 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 »

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