"Aniridia" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A congenital abnormality in which there is only a rudimentary iris. This is due to the failure of the optic cup to grow. Aniridia also occurs in a hereditary form, usually autosomal dominant.
| Descriptor ID |
D015783
|
| MeSH Number(s) |
C11.250.060 C11.270.060 C11.941.375.060 C16.131.384.079 C16.320.290.078
|
| Concept/Terms |
Aniridia- Aniridia
- Irideremia
- Absent Iris
- Congenital Aniridia
|
Below are MeSH descriptors whose meaning is more general than "Aniridia".
Below are MeSH descriptors whose meaning is more specific than "Aniridia".
This graph shows the total number of publications written about "Aniridia" by people in this website by year, and whether "Aniridia" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Aniridia" by people in Profiles.
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Aniridia: A Rare Manifestation Of Congenital Rubella Syndrome. J Ayub Med Coll Abbottabad. 2019 Jan-Mar; 31(1):131-133.
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A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome. Am J Med Genet A. 2018 06; 176(6):1427-1431.
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Mutation analysis of paired box 6 gene in inherited aniridia in northern China. Mol Vis. 2013; 19:1169-77.
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Long-term outcome of black diaphragm intraocular lens implantation in traumatic aniridia. Br J Ophthalmol. 2010 Apr; 94(4):456-9.