Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
eye disease +     
Abnormalities, Drug-Induced +   
Abnormalities, Radiation-Induced 
Abnormalities, Severe Teratoid +   
Abnormalities, Urinary Tract +   
Accessory Pancreas 
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency  
Aicardi syndrome 
Aland Island eye disease  
Amastia +   
amblyopia +   
ancylostomiasis +  
anterior segment mesenchymal dysgenesis +   
Arrhinia 
asthenopia  
Atlanto-Axial Fusion 
Aural Atresia, Congenital  
baylisascariasis 
Bile and Pancreatic Ducts, Complete Absence of 
blindness +   
Bresheck/Bresek Syndrome 
Cardiovascular Abnormalities +   
Caudal Duplication Anomaly  
chromosomal disease +   
Cogan syndrome +   
congenital diaphragmatic hernia +   
Congenital Microtia +   
conjunctival disease +   
corneal disease +   
Crane-Heise Syndrome 
cysticercosis +  
Deal Barratt Dillon Syndrome 
Digestive System Abnormalities +   
dipetalonemiasis 
Encephalocraniocutaneous Lipomatosis  
Eye Abnormalities +   
Congenital absence of or defects in structures of the eye; may also be hereditary.
eye accommodation disease +  
eye degenerative disease +   
Eye Hemorrhage +   
Eye Infections +   
Eye Injuries +   
Eye Manifestations +   
Eye Neoplasms +   
eyelid disease +   
Familial Cryptotia 
fundus dystrophy +   
Gallbladder, Agenesis Of 
glaucoma +   
globe disease +   
gonorrhea +  
Hereditary Eye Diseases +   
Hereditary Sensorimotor Neuropathy with Upper Motor Neuron, Visual Pathway and Autonomic Disturbance 
Hernandez Fragoso Syndrome 
Hydrocephalus, Skeletal Anomalies, and Mental Disturbance 
lacrimal apparatus disease +   
Laryngeal Cleft 
Laryngeal Web, Familial 
lens disease +   
leprosy +   
loiasis 
Lymphatic Abnormalities +   
Marfan syndrome +   
microphthalmia +   
Mollica Pavone Antener Syndrome 
Mondini Dysplasia  
MORM Syndrome  
Mullerian Aplasia  
Multiple Abnormalities +   
Musculoskeletal Abnormalities +   
Nasal Bones, Absence of 
Nervous System Malformations +   
ocular albinism +   
ocular hypertension +   
ocular hypotension +   
ocular motility disease +   
Ocular Neovascularization +   
ophthalmia nodosa 
ophthalmomyiasis 
optic nerve disease +   
orbital disease +   
Pancreas Agenesis, Dorsal 
Patterson Stevenson Syndrome +   
philophthalmiasis 
pupil disease +   
refractive error +   
Renal and Mullerian Duct Hypoplasia +   
Respiratory System Abnormalities +   
retinal disease +   
Rhiny 
Saito Kuba Tsuruta Syndrome 
Schlegelberger Grote Syndrome 
scleral disease +   
scotoma +  
situs inversus +   
Skin Abnormalities +   
Sprengel Deformity 
Stomatognathic System Abnormalities +   
Stridor, Congenital 
thyroid malformation +   
toxocariasis +   
Urogenital Abnormalities +   
uveal disease +   
Vagina, Absence of 
Vertebral Fusion Posterior Lumbosacral Blepharoptosis 
Vision Disorders +   
visual pathway disease +   
vitreous detachment +   
 aniridia +   
 Anophthalmia +   
 coloboma +   
 Ectopia Lentis +   
 Fraser syndrome +   
 hydrophthalmos +   
 microphthalmia +   

Synonyms
Exact Synonyms: Eye Abnormality
Primary IDs: MESH:D005124 ;   RDO:0000705
Definition Sources: MESH:D005124

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.