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Results 1 - 10 of 75 for cataract
  1. Hyperferritinemia-cataract syndrome is a disorder characterized by an excess of an iron storage protein called ferritin in the blood (hyperferritinemia) and tissues of ...
  2. Autosomal dominant optic atrophy and cataract is an eye disorder that is characterized by impaired vision. Most affected individuals have decreased sharpness of ...
  3. Hypomyelination and congenital cataract is an inherited condition that affects the nervous system and the eyes. This disease is one of a group ... rapid transmission of nerve impulses. Hypomyelination and congenital cataract is caused by a reduced ability to form ...
  4. Congenital cataracts, facial dysmorphism, and neuropathy (CCFDN) is a rare disorder that affects several parts of the body. It ...
  5. ... have clouding of the lenses of the eyes (cataracts) from birth (congenital) or beginning in infancy.CLPB ... methylglutaconic aciduria type VII 3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia 3-methylglutaconic aciduria-cataract- ...
  6. ... and clouding of the lens of the eyes (cataracts).The bleeding problems in people with MYH9-related ... stage renal disease (ESRD).Some affected individuals develop cataracts in early adulthood that worsen over time.Not ...
  7. ... a clouding of the lens of the eye (cataract), which affects vision. Many people with this disorder ... of the condition. Congenital poikiloderma Poikiloderma atrophicans and cataract Poikiloderma congenitale Poikiloderma congenitale of Rothmund-Thomson RTS ...
  8. ... or clouding of the lens of the eye (cataract). In addition, some people have breakdown (degeneration) of ... ADVIRC Vitreoretinochoroidopathy dominant Vitreoretinochoroidopathy with microcornea, glaucoma, and ... Genetic Testing Registry: ...
  9. ... eye problems can include clouding of the lens (cataract) and a higher risk of glaucoma, an eye ... males are born with OFCD syndrome. MCOPS2 Microphthalmia, cataracts, radiculomegaly, and septal heart defects Microphthalmia, syndromic 2 ...
  10. ... have been found to cause hypomyelination and congenital cataract. Most mutations delete a large portion of the ... of hyccin causes a clouding of the lens (cataract) in both eyes that is typically present from ...
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