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Anteverted nostrils and Claw hand and Eyelid symptoms and Hand symptoms and Skin texture changes and Tooth deformity
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Anteverted nostrils and Claw hand and Eyelid symptoms and Hand symptoms and Skin texture changes and Tooth deformity

  • Anteverted nostrils AND Claw hand AND Eyelid symptoms AND Hand symptoms AND Skin texture changes AND Tooth deformity - Causes of All Symptoms
  • Anteverted nostrils OR Claw hand OR Eyelid symptoms OR Hand symptoms OR Skin texture changes OR Tooth deformity - 2935 causes

Anteverted nostrils:

Claw hand:

Eyelid symptoms:

Hand symptoms:

Skin texture changes:

Tooth deformity:

Results: Causes of Anteverted nostrils AND Claw hand AND Eyelid symptoms AND Hand symptoms AND Skin texture changes AND Tooth deformity

Results: 2935 causes of Anteverted nostrils OR Claw hand OR Eyelid symptoms OR Hand symptoms OR Skin texture changes OR Tooth deformity

    1. 14qter deletion Syndrome
     A very rare genetic condition where a portion at the end of the long arm (q) of chromosome 14 is missing....more »
    2. 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 »
    3. 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 »
    4. 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 »
    5. 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 »
    6. 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 »
    7. 2p21 deletion syndrome
     This syndrome is a more severe form hypotonia-cystinuria syndrome as a larger portion of genetic material from chromosome 2p21 is deleted. It is characterized by infant seizures, reduced muscle tone, developmental delay, lactic acidosis and unusual facial...more »
    8. 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 »
    9. 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 »
    10. 3C syndrome
     A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name....more »

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