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Symptom Checker » Aches » Collagen vascular diseases causing fever
 

Aches and Collagen vascular diseases causing fever and Connective tissue numb and Food symptoms and Heart symptoms and Metacarpophalangeal joint sensitive
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Aches and Collagen vascular diseases causing fever and Connective tissue numb and Food symptoms and Heart symptoms and Metacarpophalangeal joint sensitive

  • Aches AND Collagen vascular diseases causing fever AND Connective tissue numb AND Food symptoms AND Heart symptoms AND Metacarpophalangeal joint sensitive - Causes of All Symptoms
  • Aches OR Collagen vascular diseases causing fever OR Connective tissue numb OR Food symptoms OR Heart symptoms OR Metacarpophalangeal joint sensitive - 4907 causes

Aches:

Collagen vascular diseases causing fever:

Connective tissue numb:

Food symptoms:

Heart symptoms:

Metacarpophalangeal joint sensitive:

Results: Causes of Aches AND Collagen vascular diseases causing fever AND Connective tissue numb AND Food symptoms AND Heart symptoms AND Metacarpophalangeal joint sensitive

Results: 4907 causes of Aches OR Collagen vascular diseases causing fever OR Connective tissue numb OR Food symptoms 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. 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 »
    5. 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 »
    6. 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 »
    7. 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 »
    8. 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 »
    9. 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 »
    10. 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 »

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