Structured Summary
Abstract
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.
MeSH Record
Classification
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MeSH Record
Synonyms
3 entry terms
- Absent Iris
- Congenital Aniridia
- Irideremia
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
rudimentary iris; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
MeSH Record
History Note
90
MeSH Record
Previous Indexing
- Chromosome Deletion (1975-1989)
- Iris/abnormalities (1966-1989)
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Tree Numbers
AMA Style
References
- National Library of Medicine. Aniridia. Medical Subject Headings (MeSH). 2026. Unique ID D015783. http://id.nlm.nih.gov/mesh/2026/D015783
- Aniridia. In: Wikipedia. https://en.wikipedia.org/wiki/Aniridia
- Aniridia. In: Wikidata. https://www.wikidata.org/wiki/Q548719