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Anteverted nostrils and Kyphosis and Skin texture changes and Small eye and Umbilical hernia and Vertebra symptoms
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Anteverted nostrils and Kyphosis and Skin texture changes and Small eye and Umbilical hernia and Vertebra symptoms

  • Anteverted nostrils AND Kyphosis AND Skin texture changes AND Small eye AND Umbilical hernia AND Vertebra symptoms - Causes of All Symptoms
  • Anteverted nostrils OR Kyphosis OR Skin texture changes OR Small eye OR Umbilical hernia OR Vertebra symptoms - 1428 causes

Anteverted nostrils:

Kyphosis:

Skin texture changes:

Small eye:

Umbilical hernia:

Vertebra symptoms:

Results: Causes of Anteverted nostrils AND Kyphosis AND Skin texture changes AND Small eye AND Umbilical hernia AND Vertebra symptoms

    1. Chromosome 6, monosomy 6q
     A rare chromosomal disorder where a part of the long arm (q) of chromosome 6 is deleted resulting in various abnormalities depending on the location and length of missing genetic material....read more »
    2. Chromosome 6q deletion syndrome
     A rare chromosomal disorder where a part of the long arm (q) of chromosome 6 is deleted resulting in various abnormalities depending on the location and length of missing genetic material....read more »

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Results: 1428 causes of Anteverted nostrils OR Kyphosis OR Skin texture changes OR Small eye OR Umbilical hernia OR Vertebra symptoms

    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 terminal deletion
     A rare chromosomal disorder where the terminal part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities....more »
    4. 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 »
    5. 3C syndrome
     A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name....more »
    6. 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 »
    7. 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 »
    8. 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 »
    9. 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 »
    10. Aarskog Syndrome
     A rare genetic condition characterized by facial, hand, genital and growth abnormalities....more »

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