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Symptom Checker » Anteverted nostrils » Hand symptoms
 

Anteverted nostrils and Hand symptoms and Infant symptoms and Long thin fingers and Skin texture changes and Tooth deformity
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Results: Causes of Anteverted nostrils AND Hand symptoms AND Infant symptoms AND Long thin fingers AND Skin texture changes AND Tooth deformity

Results: 4255 causes of Anteverted nostrils OR Hand symptoms OR Infant symptoms OR Long thin fingers OR Skin texture changes OR Tooth deformity

    21. 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 »
    22. 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 »
    23. 46,XX testicular DSD
     A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY....more »
    24. 46,XX testicular disorder of sex development
     A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY....more »
    25. 47 XYY syndrome
     A genetic condition where males have an extra Y chromosome in each of their cells. Normally male cells have one X and one Y chromosome. This is not usually an inherited condition but a defect that occurs during cell division. Often the condition is asympt...more »
    26. 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 »
    27. 49,XXXXX syndrome
     A rare chromosomal disorder that affects only females and involves body cells having five copies of the X chromosome instead of the normal two....more »
    28. 49,XXXXY syndrome
     A rare sex chromosome abnormality where there are three extra copies of the X chromosome....more »
    29. 4p16.3 deletion
     A rare genetic disorder where a portion of chromosome 4 is deleted at a location called 16.3. The condition is characterized by malformations in most parts of the body as the deletion affects growth and development of the fetus....more »
    30. 8p-Syndrome, partial
     A rare chromosomal disorder where there is one copy of part of the short arm (p) of chromosome 8 rather than the normal two. The type and severity of symptoms is determined by the location and size of the genetic material deleted....more »

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