Diseases

Aniridia

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.

National Library of MedicineMedical Subject Headings2026

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

Related Concepts

Knowledge Graph

Loading graph…

Drag nodes to rearrange; hover to trace links; click a node to open its page.

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)

MeSH Hierarchy

Tree Numbers

AMA Style

References

  1. National Library of Medicine. Aniridia. Medical Subject Headings (MeSH). 2026. Unique ID D015783. http://id.nlm.nih.gov/mesh/2026/D015783
  2. Aniridia. In: Wikipedia. https://en.wikipedia.org/wiki/Aniridia
  3. Aniridia. In: Wikidata. https://www.wikidata.org/wiki/Q548719