Albinism, Ocular [albinismus oční]
- Terms
-
albinismus očí
albinismus okulární
oční albinismus
okulární albinismus
-
Ocular Albinism
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.
- Annotation
- hypopigmentation of eye; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
- DUI
- D016117 MeSH Browser
- CUI
- M0024622
- Previous indexing
- Albinism (1966-1990)
- History note
- 91
- Public note
- 91
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 2
- CO
- complications
- DI
- diagnosis
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology 1
- GE
- genetics 1
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 1
- PP
- physiopathology 1
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery 1
- TH
- therapy 1
- UR
- urine
- VE
- veterinary
- VI
- virology
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Ocular Albinism type 1 Disease MeSH Browser