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Symptom Checker » Anteverted nostrils » Long thin fingers
 

Anteverted nostrils and Long thin fingers and Night blindness and Skin texture changes and Squint and Tooth deformity
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Anteverted nostrils and Long thin fingers and Night blindness and Skin texture changes and Squint and Tooth deformity

  • Anteverted nostrils AND Long thin fingers AND Night blindness AND Skin texture changes AND Squint AND Tooth deformity - Causes of All Symptoms
  • Anteverted nostrils OR Long thin fingers OR Night blindness OR Skin texture changes OR Squint OR Tooth deformity - 1148 causes

Anteverted nostrils:

Long thin fingers:

Night blindness:

Skin texture changes:

Squint:

Tooth deformity:

Results: Causes of Anteverted nostrils AND Long thin fingers AND Night blindness AND Skin texture changes AND Squint AND Tooth deformity

Results: 1148 causes of Anteverted nostrils OR Long thin fingers OR Night blindness OR Skin texture changes OR Squint OR Tooth deformity

    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. 3C syndrome
     A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name....more »
    4. 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 »
    5. 49,XXXXY syndrome
     A rare sex chromosome abnormality where there are three extra copies of the X chromosome....more »
    6. 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 »
    7. Aarskog Syndrome
     A rare genetic condition characterized by facial, hand, genital and growth abnormalities....more »
    8. Ablepharon macrostomia syndrome
     A rare disorder involving a number of mainly physical abnormalities....more »
    9. Accessory navicular bone
     An abnormal bone that develops in the arch in the middle of the foot. Often there are no symptoms but if the bone is large it may rub against shoes and cause problems....more »
    10. Achondrogenesis type 2
     A rare genetic disorder characterized by very small stature, abnormal bone formation and early death....more »

    More causes » | Show All 1148 Causes
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Notes About Causes

  • Warning - Beta version - information may be incorrect (details)
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