Eye Abnormalities [abnormality očí]
- Terms
-
oči - abnormality
Congenital absence of or defects in structures of the eye; may also be hereditary.
- Annotation
- do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; these are structural abnorm: EYE DISEASES, HEREDITARY is also available
- DUI
- D005124 MeSH Browser
- CUI
- M0008084
- Previous indexing
- Eye/abnormalities (1977-1989); specific eye heading/abnormalities (1977-1989)
- History note
- 90; was NON MESH 1977-89
- Public note
- 90
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced 1
- CL
- classification 9
- CO
- complications 4
- DI
- diagnosis 14
- DG
- diagnostic imaging 2
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology 1
- EN
- enzymology 2
- EP
- epidemiology 1
- EH
- ethnology
- ET
- etiology 14
- GE
- genetics 17
- HI
- history
- IM
- immunology
- ME
- metabolism 1
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 12
- PP
- physiopathology 1
- PC
- prevention & control 1
- PX
- psychology 1
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery 9
- TH
- therapy 14
- UR
- urine
- VE
- veterinary
- VI
- virology
Ablepharon macrostomia syndrome Disease MeSH Browser
Agenesis of Cerebellar Vermis Disease MeSH Browser
Ankyloblepharon filiforme adnatum Disease MeSH Browser
Anterior segment mesenchymal dysgenesis Disease MeSH Browser
Asymmetric Short Stature Syndrome Disease MeSH Browser
Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities Disease MeSH Browser
Axenfeld-Rieger anomaly with cardiac defects and sensorineural hearing loss Disease MeSH Browser
Axenfeld-Rieger syndrome Disease MeSH Browser
Blue diaper syndrome Disease MeSH Browser
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism Disease MeSH Browser
Brittle cornea syndrome 1 Disease MeSH Browser
CODAS syndrome Disease MeSH Browser
Chemke Oliver Mallek syndrome Disease MeSH Browser
Chromosome 6pter-P24 Deletion Syndrome Disease MeSH Browser
Cole Carpenter syndrome Disease MeSH Browser
Craniosynostosis with Ocular Abnormalities and Hallucal Defects Disease MeSH Browser
Cryptophthalmos, Unilateral or Bilateral, Isolated Disease MeSH Browser
Dwarfism stiff joint ocular abnormalities Disease MeSH Browser
FACES syndrome Disease MeSH Browser
Foveal Hypoplasia and Anterior Segment Dysgenesis Disease MeSH Browser
Fronto-facio-nasal dysplasia Disease MeSH Browser
Frontoocular Syndrome Disease MeSH Browser
Goniodysgenesis-Mental Retardation-Short Stature Syndrome Disease MeSH Browser
Hay-Wells syndrome Disease MeSH Browser
Iridogoniodysgenesis and skeletal anomalies Disease MeSH Browser
Iridogoniodysgenesis type1 Disease MeSH Browser
Iridogoniodysgenesis, dominant type Disease MeSH Browser
Jejunal Atresia with Microcephaly and Ocular Anomalies Disease MeSH Browser
Joubert Syndrome 9 Disease MeSH Browser
Joubert syndrome 2 Disease MeSH Browser
Kapur Toriello syndrome Disease MeSH Browser
Kaufman oculocerebrofacial syndrome Disease MeSH Browser
MOMES Syndrome Disease MeSH Browser
Macrophthalmia, Colobomatous, with Microcornea Disease MeSH Browser
Maxillofacial Dysostosis Disease MeSH Browser
Mesangial Sclerosis, Diffuse Renal, with Ocular Abnormalities Disease MeSH Browser
Microcornea, glaucoma, and absent frontal sinuses Disease MeSH Browser
Nephrotic Syndrome, Congenital, with or without Ocular Abnormalities Disease MeSH Browser
Nephrotic syndrome ocular anomalies Disease MeSH Browser
Oculoauricular Syndrome Disease MeSH Browser
Oculoauriculofrontonasal syndrome Disease MeSH Browser
Oculocerebrocutaneous syndrome Disease MeSH Browser
Oculodentodigital Dysplasia Disease MeSH Browser
Oculodentodigital Dysplasia, Autosomal Recessive Disease MeSH Browser
Oculomaxillofacial dysostosis Disease MeSH Browser
Oculopalatocerebral Syndrome Disease MeSH Browser
Oculopalatoskeletal syndrome Disease MeSH Browser
Oculorenocerebellar syndrome Disease MeSH Browser
PHACE association Disease MeSH Browser
Pena Shokeir syndrome Type 2 Disease MeSH Browser
Persistent Hyperplastic Primary Vitreous, Autosomal Recessive Disease MeSH Browser
Peters anomaly Disease MeSH Browser
Popliteal Pterygium Syndrome Disease MeSH Browser
Popliteal Pterygium Syndrome, Lethal Type Disease MeSH Browser
Prepapillary Vascular Loops Disease MeSH Browser
Pupil, Egg-Shaped Disease MeSH Browser
Pupillary Membrane, Persistence Of Disease MeSH Browser
Rieger syndrome 2 Disease MeSH Browser
Rozin Hertz Goodman syndrome Disease MeSH Browser
Schmid-Fraccaro syndrome Disease MeSH Browser
Torsion dystonia with onset in infancy Disease MeSH Browser