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Eye Abnormalities
MeSH Descriptor Data 2025
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Eye Abnormalities
Tree Number(s)
C11.250
C16.131.384
Unique ID
D005124
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D005124
Annotation
do not use
/congen
& do not coord with
INFANT, NEWBORN, DISEASES
; these are structural abnorm:
EYE DISEASES, HEREDITARY
is also available
Scope Note
Congenital absence of or defects in structures of the eye; may also be hereditary.
Entry Version
EYE ABNORM
NLM Classification #
WW 101
Previous Indexing
Eye/abnormalities (1977-1989)
specific eye heading/abnormalities (1977-1989)
Public MeSH Note
90
History Note
90; was NON MESH 1977-89
Date Established
1990/01/01
Date of Entry
1999/01/01
Revision Date
1999/11/03
Allowable Qualifiers
blood (BL)
cerebrospinal fluid (CF)
chemically induced (CI)
classification (CL)
complications (CO)
diagnosis (DI)
diagnostic imaging (DG)
diet therapy (DH)
drug therapy (DT)
economics (EC)
embryology (EM)
enzymology (EN)
epidemiology (EP)
ethnology (EH)
etiology (ET)
genetics (GE)
history (HI)
immunology (IM)
metabolism (ME)
microbiology (MI)
mortality (MO)
nursing (NU)
parasitology (PS)
pathology (PA)
physiopathology (PP)
prevention & control (PC)
psychology (PX)
radiotherapy (RT)
rehabilitation (RH)
surgery (SU)
therapy (TH)
urine (UR)
veterinary (VE)
virology (VI)
Eye Diseases [C11]
Asthenopia [C11.093]
Cogan Syndrome [C11.180]
Conjunctival Diseases [C11.187]
Corneal Diseases [C11.204]
Eye Abnormalities [C11.250]
Aniridia [C11.250.060]
Anophthalmos [C11.250.080]
Blepharophimosis [C11.250.090]
Choroidal Effusions [C11.250.105]
Coloboma [C11.250.110]
Ectopia Lentis [C11.250.300]
Familial Exudative Vitreoretinopathies [C11.250.345]
Fraser Syndrome [C11.250.390]
Hydrophthalmos [C11.250.480]
Microphthalmos [C11.250.566]
Persistent Hyperplastic Primary Vitreous [C11.250.616]
Retinal Dysplasia [C11.250.666]
Eye Diseases, Hereditary [C11.270]
Eye Hemorrhage [C11.290]
Eye Infections [C11.294]
Eye Injuries [C11.297]
Eye Manifestations [C11.300]
Eye Neoplasms [C11.319]
Eyelid Diseases [C11.338]
Lacrimal Apparatus Diseases [C11.496]
Lens Diseases [C11.510]
Ocular Hypertension [C11.525]
Ocular Hypotension [C11.540]
Ocular Motility Disorders [C11.590]
Optic Nerve Diseases [C11.640]
Orbital Diseases [C11.675]
Pupil Disorders [C11.710]
Refractive Errors [C11.744]
Retinal Diseases [C11.768]
Scleral Diseases [C11.790]
Uveal Diseases [C11.941]
Vision Disorders [C11.966]
Vitreous Detachment [C11.980]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Drug-Induced [C16.131.042]
Abnormalities, Multiple [C16.131.077]
Abnormalities, Radiation-Induced [C16.131.080]
Abnormalities, Severe Teratoid [C16.131.085]
Aicardi Syndrome [C16.131.162]
Cardiovascular Abnormalities [C16.131.240]
Chromosome Disorders [C16.131.260]
Congenital Microtia [C16.131.287]
Digestive System Abnormalities [C16.131.314]
Eye Abnormalities [C16.131.384]
Aniridia [C16.131.384.079]
Anophthalmos [C16.131.384.159]
Blepharophimosis [C16.131.384.190]
Coloboma [C16.131.384.282]
Ectopia Lentis [C16.131.384.405]
Familial Exudative Vitreoretinopathies [C16.131.384.424]
Fraser Syndrome [C16.131.384.442]
Hydrophthalmos [C16.131.384.480]
Microphthalmos [C16.131.384.666]
Persistent Hyperplastic Primary Vitreous [C16.131.384.725]
Retinal Dysplasia [C16.131.384.784]
Hernias, Diaphragmatic, Congenital [C16.131.433]
Lymphatic Abnormalities [C16.131.482]
Musculoskeletal Abnormalities [C16.131.621]
Nervous System Malformations [C16.131.666]
Respiratory System Abnormalities [C16.131.740]
Situs Inversus [C16.131.810]
Skin Abnormalities [C16.131.831]
Stomatognathic System Abnormalities [C16.131.850]
Thyroid Dysgenesis [C16.131.894]
Urogenital Abnormalities [C16.131.939]
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Eye Abnormalities
Preferred
Concept UI
M0008084
Scope Note
Congenital absence of or defects in structures of the eye; may also be hereditary.
Terms
Eye Abnormalities
Preferred Term
Term UI
T015684
Date
01/01/1999
LexicalTag
NON
ThesaurusID
NLM (1990)
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