Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 29 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 optic nerve Retinochoroidal coloboma 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. FOXC1 gene 
    ... especially affecting the eye. Abnormal formation of the iris, cornea, and other structures of the anterior segment leads to the features of Peters anomaly. The FOXC1 gene mutations that cause Peters anomaly can cause other related eye disorders, such as Axenfeld-Rieger syndrome (described above), in ...
    https://medlineplus.gov/genetics/gene/foxc1 - Genetics
  5. 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
  6. 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
  7. Is eye color determined by genetics?: MedlinePlus Genetics 
    ... relatives, genetic variations sometimes produce unexpected results. Several disorders that affect eye color have been described. Ocular albinism is characterized by severely reduced pigmentation of the iris, which causes very light-colored eyes and significant ...
    https://medlineplus.gov/genetics/understanding/traits/eyecolor - Genetics
  8. 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
  9. 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
  10. 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
previous · 1 · 2 · 3 · next