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Symptom Checker » Anteverted nostrils » Hand symptoms
 

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

  • Anteverted nostrils AND Hand symptoms AND Long thin fingers AND Ocular weakness AND Skin texture changes AND Wide-set eyes - Causes of All Symptoms
  • Anteverted nostrils OR Hand symptoms OR Long thin fingers OR Ocular weakness OR Skin texture changes OR Wide-set eyes - 2637 causes

Anteverted nostrils:

Hand symptoms:

Long thin fingers:

Ocular weakness:

Skin texture changes:

Wide-set eyes:

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

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

Results: 2637 causes of Anteverted nostrils OR Hand symptoms OR Long thin fingers OR Ocular weakness OR Skin texture changes OR Wide-set eyes

    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-M Syndrome
     A rare genetic condition which is characterized by distinctive physical features and severe growth retardation that starts during the fetal stage. Intelligence is not affected....more »
    7. 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 »
    8. 3C syndrome
     A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name....more »
    9. 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 »
    10. 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 »

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Notes About Causes

  • Warning - Beta version - information may be incorrect (details)
  • Disclaimer - Do not use this information for diagnosis (details)
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