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Anteverted nostrils and Hand symptoms and Long thin fingers and Night blindness and Skeletal symptoms and Skin texture changes
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Anteverted nostrils and Hand symptoms and Long thin fingers and Night blindness and Skeletal symptoms and Skin texture changes

  • Anteverted nostrils AND Hand symptoms AND Long thin fingers AND Night blindness AND Skeletal symptoms AND Skin texture changes - Causes of All Symptoms
  • Anteverted nostrils OR Hand symptoms OR Long thin fingers OR Night blindness OR Skeletal symptoms OR Skin texture changes - 4975 causes

Anteverted nostrils:

Hand symptoms:

Long thin fingers:

Night blindness:

Skeletal symptoms:

Skin texture changes:

Results: Causes of Anteverted nostrils AND Hand symptoms AND Long thin fingers AND Night blindness AND Skeletal symptoms AND Skin texture changes

Results: 4975 causes of Anteverted nostrils OR Hand symptoms OR Long thin fingers OR Night blindness OR Skeletal symptoms OR Skin texture changes

    1. 14q+ syndrome
     A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....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. 2-Hydroxyglutaricaciduria
     A rare metabolic disorder characterized by high levels of a certain chemical (2-Hydroxyglutaric) which causes a serious progressive neurological disease and damage to the brain. The features of this disorder are variable and some cases are milder than oth...more »
    7. 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 »
    8. 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 »
    9. 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 »
    10. 2q22-q24 deletion
     A rare chromosomal disorder where part of the long arm (q22-q24) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »

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