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Symptom Checker » Anteverted nostrils » Communication symptoms
 

Anteverted nostrils and Communication symptoms and Dental symptoms and Hand symptoms and Long thin fingers and Skin texture changes
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Anteverted nostrils and Communication symptoms and Dental symptoms and Hand symptoms and Long thin fingers and Skin texture changes

  • Anteverted nostrils AND Communication symptoms AND Dental symptoms AND Hand symptoms AND Long thin fingers AND Skin texture changes - Causes of All Symptoms
  • Anteverted nostrils OR Communication symptoms OR Dental symptoms OR Hand symptoms OR Long thin fingers OR Skin texture changes - 3918 causes

Anteverted nostrils:

Communication symptoms:

Dental symptoms:

Hand symptoms:

Long thin fingers:

Skin texture changes:

Results: Causes of Anteverted nostrils AND Communication symptoms AND Dental symptoms AND Hand symptoms AND Long thin fingers AND Skin texture changes

Results: 3918 causes of Anteverted nostrils OR Communication symptoms OR Dental symptoms OR Hand symptoms OR Long thin fingers OR Skin texture changes

    1. 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 »
    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 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 »
    4. 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 »
    5. 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 »
    6. 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency
     A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Sympt...more »
    7. 3-methylglutaconic aciduria, type 1
     A recessively inherited metabolic disorder characterized by methylglutaconic acid in the urine....more »
    8. 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 »
    9. 3C syndrome
     A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name....more »
    10. 3q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 3 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »

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