 Iris Diseases
"Iris Diseases" 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.
Diseases, dysfunctions, or disorders of or located in the iris.
| Descriptor ID |
D007499
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| MeSH Number(s) |
C11.941.375
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| Concept/Terms |
Iris Diseases- Iris Diseases
- Disease, Iris
- Diseases, Iris
- Iris Disease
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Below are MeSH descriptors whose meaning is more general than "Iris Diseases".
Below are MeSH descriptors whose meaning is more specific than "Iris Diseases".
This graph shows the total number of publications written about "Iris Diseases" by people in this website by year, and whether "Iris Diseases" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 0 | 1 | 1 | | 2011 | 0 | 1 | 1 | | 2017 | 0 | 1 | 1 |
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Below are the most recent publications written about "Iris Diseases" by people in Profiles.
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Smith JM, Hwang RY, Siringo F, Quiroz-Mercado H, Oliver SC, Mandava N, Mathias MT, Olson JL. CONCURRENT ENDOPHTHALMITIS AND ANTERIOR SEGMENT ISCHEMIA AFTER STRABISMUS SURGERY. Retin Cases Brief Rep. 2017 Spring; 11(2):148-151.
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Cyr AB, Nimmakayalu M, Longmuir SQ, Patil SR, Keppler-Noreuil KM, Shchelochkov OA. A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features. Am J Med Genet A. 2011 Sep; 155A(9):2224-8.
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Heys JJ, Barocas VH, Taravella MJ. Modeling passive mechanical interaction between aqueous humor and iris. J Biomech Eng. 2001 Dec; 123(6):540-7.
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Morell R, Spritz RA, Ho L, Pierpont J, Guo W, Friedman TB, Asher JH. Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism (AROA). Hum Mol Genet. 1997 May; 6(5):659-64.
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