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Results 1 - 10 of 23 for Iris disorder
  1. Aniridia 
    ... occur in people with no history of the disorder in their family. Absent iris Congenital aniridia Irideremia Genetic Testing Registry: Aniridia 1 Genetic Testing Registry: Congenital aniridia Isolated aniridia National Organization for Rare Disorders (NORD) ... ANIRIDIA 1; AN1 PubMed Chao ...
    https://medlineplus.gov/genetics/condition/aniridia - Genetics
  2. Coloboma 
    ... Testing Registry: Coloboma, ocular, autosomal recessive Coloboma of iris Coloboma of choroid and retina National Organization for Rare Disorders (NORD) ClinicalTrials.gov MICROPHTHALMIA/COLOBOMA 12; MCOPCB12 COLOBOMA, ...
    https://medlineplus.gov/genetics/condition/coloboma - Genetics
  3. Baraitser-Winter syndrome 
    ... occurs in people with no history of the disorder in their family. BRWS Cerebro-frontofacial syndrome, type 3 Fryns-Aftimos syndrome Iris coloboma with ptosis, hypertelorism, and mental retardation Genetic ...
    https://medlineplus.gov/genetics/condition/baraitser-winter-syndrome - Genetics
  4. Constitutional mismatch repair deficiency syndrome 
    ... in the colored part of the eye (the iris). Lisch nodules do not interfere with vision. Some people with CMMRD syndrome are initially misdiagnosed with neurofibromatosis type 1. CMMRD syndrome is a rare disorder; more than 200 affected individuals have been reported ...
    https://medlineplus.gov/...ional-mismatch-repair-deficiency-syndrome - Genetics
  5. Horner syndrome 
    ... and a bloodshot eye often occur in this disorder. In people with Horner syndrome that occurs before the age of 2, the colored part (iris) of the eyes may differ in color (iris ...
    https://medlineplus.gov/genetics/condition/horner-syndrome - Genetics
  6. Peters anomaly 
    ... by an incomplete separation of the cornea and iris and mild to moderate corneal opacity. Type ... is one of a group of disorders known as congenital corneal opacities, which affect 3 ...
    https://medlineplus.gov/genetics/condition/peters-anomaly - Genetics
  7. Hermansky-Pudlak syndrome 
    ... white or light-colored hair. People with this disorder have a higher than average risk of skin damage and skin cancers caused by long-term sun exposure. Oculocutaneous albinism reduces pigmentation of the colored part of the eye (iris) and the light-sensitive tissue at the back ...
    https://medlineplus.gov/genetics/condition/hermansky-pudlak-syndrome - Genetics
  8. Tietz syndrome 
    ... eyes. The colored part of the eye (the iris) in affected individuals is blue, and ... Tietz syndrome is a rare disorder; its exact prevalence is unknown. Only a few ...
    https://medlineplus.gov/genetics/condition/tietz-syndrome - Genetics
  9. Gillespie syndrome 
    Gillespie syndrome is a disorder ... of the iris is missing (partial aniridia) in both eyes. In addition, the irises have ...
    https://medlineplus.gov/genetics/condition/gillespie-syndrome - Genetics
  10. Axenfeld-Rieger syndrome 
    Axenfeld-Rieger syndrome is primarily ... has a single central hole, called the pupil, through which light enters the eye. ...
    https://medlineplus.gov/genetics/condition/axenfeld-rieger-syndrome - Genetics
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