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Enophthalmos and Eye symptoms and Head symptoms and Retina symptoms and Sunken eyes and Vision distortion
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Enophthalmos and Eye symptoms and Head symptoms and Retina symptoms and Sunken eyes and Vision distortion

  • Enophthalmos AND Eye symptoms AND Head symptoms AND Retina symptoms AND Sunken eyes AND Vision distortion - Causes of All Symptoms
  • Enophthalmos OR Eye symptoms OR Head symptoms OR Retina symptoms OR Sunken eyes OR Vision distortion - 9823 causes

Enophthalmos:

Eye symptoms:

Head symptoms:

Retina symptoms:

Sunken eyes:

Vision distortion:

Results: Causes of Enophthalmos AND Eye symptoms AND Head symptoms AND Retina symptoms AND Sunken eyes AND Vision distortion

    1. Exudative retinopathy familial, X-linked, recessive
     A rare progressive eye disorder which is inherited in a recessive X-linked manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function. The disorder is ca...read more »
    2. Exudative retinopathy familial, autosomal dominant
     A rare progressive eye disorder which is inherited in a dominant manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function. The disorder is caused by a ...read more »
    3. Exudative retinopathy familial, autosomal recessive
     A rare progressive eye disorder which is inherited in a recessive manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function....read more »
    4. Exudative retinopathy, familial
     A rare progressive eye disorder which is inherited in a familial manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function....read more »
    5. Exudative vitreoretinopathy 3
     A rare progressive eye disorder caused by a genetic defect on chromosome 11p13-p12. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function....read more »
    6. Exudative vitreoretinopathy 4
     A rare progressive eye disorder caused by a genetic defect on chromosome 11q13.4. It can be inherited in a dominant or recessive manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels wh...read more »

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Results: 9823 causes of Enophthalmos OR Eye symptoms OR Head symptoms OR Retina symptoms OR Sunken eyes OR Vision distortion

    1. 10q Partial Trisomy
     A very rare genetic disorder characterized by the duplication of genetic material from the long arm (q) of chromosome 10 - the genetic material occurs three times in body cells instead of the normal two. The type and severity of symptoms may vary consider...more »
    2. 14q+ syndrome
     A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....more »
    3. 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 »
    4. 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 »
    5. 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 »
    6. 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 »
    7. 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 »
    8. 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 »
    9. 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 »
    10. 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 »

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