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Symptom Checker » Circulation symptoms » Dislocated hip
 

Circulation symptoms and Dislocated hip and Retina symptoms and Skeletal symptoms and Vision distortion and Weak skin
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Circulation symptoms and Dislocated hip and Retina symptoms and Skeletal symptoms and Vision distortion and Weak skin

  • Circulation symptoms AND Dislocated hip AND Retina symptoms AND Skeletal symptoms AND Vision distortion AND Weak skin - Causes of All Symptoms
  • Circulation symptoms OR Dislocated hip OR Retina symptoms OR Skeletal symptoms OR Vision distortion OR Weak skin - 6529 causes

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Dislocated hip:

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Results: Causes of Circulation symptoms AND Dislocated hip AND Retina symptoms AND Skeletal symptoms AND Vision distortion AND Weak skin

    1. Ehlers-Danlos syndrome type VI
     A rare genetic connective tissue disorder characterized by lax joints, scoliosis and fragile sclera of the eye - Ehlers Danlos type with predominant ocular abnormalities....read more »
    2. Ehlers-Danlos syndrome, 6B
     A rare genetic connective tissue disorder characterized by lax joints, scoliosis and fragile sclera of the eye - Ehlers Danlos type with predominant ocular abnormalities but lysyl-hydroxylase activity is normal1....read more »
    3. Ehlers-Danlos syndrome, kyphoscoliosis type
     A rare genetic connective tissue disorder caused by deficiency of the lysyl hydroxylase enzyme and is characterized by progressive scoliosis and muscle weakness and fragile sclera - previously known as EDS type 6....read more »

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Results: 6529 causes of Circulation symptoms OR Dislocated hip OR Retina symptoms OR Skeletal symptoms OR Vision distortion OR Weak skin

    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. 2-Methylbutyric Aciduria
     A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...more »
    8. 2-methylbutyryl-coenzyme A dehydrogenase deficiency
     A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...more »
    9. 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 »
    10. 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 »

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