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

  • Anteverted nostrils AND Dental symptoms AND Hand symptoms AND Long thin fingers AND Skin texture changes AND Squint - Causes of All Symptoms
  • Anteverted nostrils OR Dental symptoms OR Hand symptoms OR Long thin fingers OR Skin texture changes OR Squint - 3064 causes

Anteverted nostrils:

Dental symptoms:

Hand symptoms:

Long thin fingers:

Skin texture changes:

Squint:

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

Results: 3064 causes of Anteverted nostrils OR Dental symptoms OR Hand symptoms OR Long thin fingers OR Skin texture changes OR Squint

    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-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. 3C syndrome
     A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name....more »
    8. 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 »
    9. 46,XX chromosome 7 deletion p13
     A chromosomal disorder where a small portion of chromosome 7 is deleted which results in a range of abnormalities....more »
    10. 47,XXX syndrome
     A genetic condition where females have an extra X chromosome in each of their cells. Normally female cells have two X chromosomes. This is not usually an inherited condition but a defect that occurs during cell division. Often the condition is asymptomati...more »

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