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Anteverted nostrils and Clubfoot and Hand symptoms and Infant symptoms and Skin texture changes and Tooth deformity
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Anteverted nostrils and Clubfoot and Hand symptoms and Infant symptoms and Skin texture changes and Tooth deformity

  • Anteverted nostrils AND Clubfoot AND Hand symptoms AND Infant symptoms AND Skin texture changes AND Tooth deformity - Causes of All Symptoms
  • Anteverted nostrils OR Clubfoot OR Hand symptoms OR Infant symptoms OR Skin texture changes OR Tooth deformity - 4342 causes

Anteverted nostrils:

Clubfoot:

Hand symptoms:

Infant symptoms:

Skin texture changes:

Tooth deformity:

Results: Causes of Anteverted nostrils AND Clubfoot AND Hand symptoms AND Infant symptoms AND Skin texture changes AND Tooth deformity

Results: 4342 causes of Anteverted nostrils OR Clubfoot OR Hand symptoms OR Infant symptoms OR Skin texture changes OR Tooth deformity

    1. +r(1) and +r(16)
     A very rare chromosomal disorder where some of the body's cells has extra ring chromosomes of chromosome 1 and chromosome 16....more »
    2. 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 »
    3. 14q+ syndrome
     A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....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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