Structured Summary
Abstract
Albinism affecting the eye in which pigment of the hair and skin is normal or only slightly diluted. The classic type is X-linked (Nettleship-Falls), but an autosomal recessive form also exists. Ocular abnormalities may include reduced pigmentation of the iris, nystagmus, photophobia, strabismus, and decreased visual acuity.
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Synonyms
1 entry terms
- Albinism, Ocular
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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
hypopigmentation of eye; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
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History Note
91
MeSH Record
Previous Indexing
- Albinism (1966-1990)
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References
- National Library of Medicine. Ocular Albinism. Medical Subject Headings (MeSH). 2026. Unique ID D016117. http://id.nlm.nih.gov/mesh/2026/D016117
- Ocular Albinism. In: Wikipedia. https://en.wikipedia.org/wiki/Ocular_albinism
- Ocular Albinism. In: Wikidata. https://www.wikidata.org/wiki/Q2831905