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Anteverted nostrils and Hand symptoms and Long thin fingers and Musculoskeletal symptoms and Skin texture changes and Wide-set eyes
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Anteverted nostrils and Hand symptoms and Long thin fingers and Musculoskeletal symptoms and Skin texture changes and Wide-set eyes

  • Anteverted nostrils AND Hand symptoms AND Long thin fingers AND Musculoskeletal symptoms AND Skin texture changes AND Wide-set eyes - Causes of All Symptoms
  • Anteverted nostrils OR Hand symptoms OR Long thin fingers OR Musculoskeletal symptoms OR Skin texture changes OR Wide-set eyes - 7436 causes

Anteverted nostrils:

Hand symptoms:

Long thin fingers:

Musculoskeletal symptoms:

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Wide-set eyes:

Results: Causes of Anteverted nostrils AND Hand symptoms AND Long thin fingers AND Musculoskeletal symptoms AND Skin texture changes AND Wide-set eyes

Results: 7436 causes of Anteverted nostrils OR Hand symptoms OR Long thin fingers OR Musculoskeletal symptoms OR Skin texture changes OR Wide-set eyes

    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. 14qter deletion Syndrome
     A very rare genetic condition where a portion at the end of the long arm (q) of chromosome 14 is missing....more »
    4. 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 »
    5. 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 »
    6. 1q proximal deletion
     A rare chromosomal disorder where the proximal part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities....more »
    7. 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 »
    8. 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 »
    9. 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 »
    10. 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 »

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