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Symptom Checker » Arm symptoms » Daytime tiredness in pregnancy
 

Arm symptoms and Daytime tiredness in pregnancy and Itching skin and Myopathy and Tiredness
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Arm symptoms and Daytime tiredness in pregnancy and Itching skin and Myopathy and Tiredness

  • Arm symptoms AND Daytime tiredness in pregnancy AND Itching skin AND Myopathy AND Tiredness - Causes of All Symptoms
  • Arm symptoms OR Daytime tiredness in pregnancy OR Itching skin OR Myopathy OR Tiredness - 3248 causes

Arm symptoms:

Daytime tiredness in pregnancy:

Itching skin:

Myopathy:

Tiredness:

Results: Causes of Arm symptoms AND Daytime tiredness in pregnancy AND Itching skin AND Myopathy AND Tiredness

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

Results: 3248 causes of Arm symptoms OR Daytime tiredness in pregnancy OR Itching skin OR Myopathy OR Tiredness

    1. 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 »
    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. 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. 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 »
    5. 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency
     A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Sympt...more »
    6. 3-methylglutaconic aciduria, type 1
     A recessively inherited metabolic disorder characterized by methylglutaconic acid in the urine....more »
    7. 3q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 3 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    8. 46,XX chromosome 7 deletion p13
     A chromosomal disorder where a small portion of chromosome 7 is deleted which results in a range of abnormalities....more »
    9. 47,XXX syndrome
     A genetic condition where females have an extra X chromosome in each of their cells. Normally female cells have two X chromosomes. This is not usually an inherited condition but a defect that occurs during cell division. Often the condition is asymptomati...more »
    10. 49,XXXXX syndrome
     A rare chromosomal disorder that affects only females and involves body cells having five copies of the X chromosome instead of the normal two....more »

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