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Symptom Checker » Aches » Collagen vascular diseases causing fever
 

Aches and Collagen vascular diseases causing fever and Difficulty rising from a chair and Heart symptoms and Metacarpophalangeal joint sensitive
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Aches and Collagen vascular diseases causing fever and Difficulty rising from a chair and Heart symptoms and Metacarpophalangeal joint sensitive

  • Aches AND Collagen vascular diseases causing fever AND Difficulty rising from a chair AND Heart symptoms AND Metacarpophalangeal joint sensitive - Causes of All Symptoms
  • Aches OR Collagen vascular diseases causing fever OR Difficulty rising from a chair OR Heart symptoms OR Metacarpophalangeal joint sensitive - 3566 causes

Aches:

Collagen vascular diseases causing fever:

Difficulty rising from a chair:

Heart symptoms:

Metacarpophalangeal joint sensitive:

Results: Causes of Aches AND Collagen vascular diseases causing fever AND Difficulty rising from a chair AND Heart symptoms AND Metacarpophalangeal joint sensitive

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

Results: 3566 causes of Aches OR Collagen vascular diseases causing fever OR Difficulty rising from a chair OR Heart symptoms OR Metacarpophalangeal joint sensitive

    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. 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 »
    4. 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 »
    5. 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 »
    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 1
     A recessively inherited metabolic disorder characterized by methylglutaconic acid in the urine....more »
    9. 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 »
    10. 3-methylglutaconic aciduria, type V
     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....more »

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  • Warning - Beta version - information may be incorrect (details)
  • Disclaimer - Do not use this information for diagnosis (details)
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