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Bone symptoms and Connective tissue blister and Connective tissue deformity and Coracobrachialis weakness and Coughing and Upper abdominal symptoms
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Bone symptoms and Connective tissue blister and Connective tissue deformity and Coracobrachialis weakness and Coughing and Upper abdominal symptoms

  • Bone symptoms AND Connective tissue blister AND Connective tissue deformity AND Coracobrachialis weakness AND Coughing AND Upper abdominal symptoms - Causes of All Symptoms
  • Bone symptoms OR Connective tissue blister OR Connective tissue deformity OR Coracobrachialis weakness OR Coughing OR Upper abdominal symptoms - 5135 causes

Bone symptoms:

Connective tissue blister:

Connective tissue deformity:

Coracobrachialis weakness:

Coughing:

Upper abdominal symptoms:

Results: Causes of Bone symptoms AND Connective tissue blister AND Connective tissue deformity AND Coracobrachialis weakness AND Coughing AND Upper abdominal symptoms

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

Results: 5135 causes of Bone symptoms OR Connective tissue blister OR Connective tissue deformity OR Coracobrachialis weakness OR Coughing 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. 14q+ syndrome
     A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....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. 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 »
    8. 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 »
    9. 2q22-q24 deletion
     A rare chromosomal disorder where part of the long arm (q22-q24) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....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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  • Warning - Beta version - information may be incorrect (details)
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