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Connective tissue blister and Coughing and Light sensitivity symptoms and Upper abdominal symptoms
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Connective tissue blister and Coughing and Light sensitivity symptoms and Upper abdominal symptoms

  • Connective tissue blister AND Coughing AND Light sensitivity symptoms AND Upper abdominal symptoms - Causes of All Symptoms
  • Connective tissue blister OR Coughing OR Light sensitivity symptoms OR Upper abdominal symptoms - 3168 causes

Connective tissue blister:

Coughing:

Light sensitivity symptoms:

Upper abdominal symptoms:

Results: Causes of Connective tissue blister AND Coughing AND Light sensitivity symptoms AND Upper abdominal symptoms

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

Results: 3168 causes of Connective tissue blister OR Coughing OR Light sensitivity symptoms OR Upper abdominal 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. 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. 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 »
    5. 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 »
    6. 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 »
    7. 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 »
    8. Aagenaes syndrome
     A rare inherited birth abnormality involving underdeveloped lymph vessels which results in swollen legs and liver problems....more »
    9. Abdominal Cancer
     Growth of abnormal cells (tumour) affecting the organs in the abdominal cavity; may be due to primary growth of a tumour or spread from another tumour (metastases, secondary tumour)...more »
    10. Abdominal Neoplasms
     A tumor that occurs in the abdomen....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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