Structured Summary
Abstract
Congenital, often bilateral, retinal abnormality characterized by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary.
MeSH Record
Classification
Broader headings
Related Concepts
Knowledge Graph
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MeSH Record
Synonyms
3 entry terms
- Dysplasia, Retinal
- Dysplasias, Retinal
- Retinal Dysplasias
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
do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
MeSH Record
History Note
90
MeSH Record
Previous Indexing
- Retina/abnormalities (1966-1989)
- Retinal Degeneration (1970-1989)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Retinal Dysplasia. Medical Subject Headings (MeSH). 2026. Unique ID D015792. http://id.nlm.nih.gov/mesh/2026/D015792
- Retinal Dysplasia. In: Wikipedia. https://en.wikipedia.org/wiki/Retinal_dysplasia
- Retinal Dysplasia. In: Wikidata. https://www.wikidata.org/wiki/Q7316763