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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
eye disease +     
Abnormalities, Drug-Induced +   
Abnormalities, Radiation-Induced 
Abnormalities, Severe Teratoid +   
Absence of Nasal Bones 
Absence of Vagina 
Accessory Pancreas 
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency  
Aicardi syndrome 
Aland Island eye disease  
Amastia +   
amblyopia +   
ancylostomiasis +  
Arrhinia 
Asthenopia  
Atlanto-Axial Fusion 
baylisascariasis 
Bile and Pancreatic Ducts, Complete Absence of 
blindness +   
Bresheck/Bresek Syndrome 
Cardiovascular Abnormalities +   
Caudal Duplication Anomaly  
Cerebellar, Ocular, Craniofacial, and Genital Syndrome  
chromosomal disease +   
Cogan syndrome +   
Congenital Aural Atresia  
congenital diaphragmatic hernia +   
Congenital Microtia +   
Congenital Stridor 
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 +   
Nervous System Malformations +   
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES  
NEUROMUSCULAR DISEASE AND OCULAR OR AUDITORY ANOMALIES WITH OR WITHOUT SEIZURES  
ocular albinism +   
ocular hypertension +   
ocular hypotension +   
ocular motility disease +   
Ocular Neovascularization +   
ophthalmia nodosa 
ophthalmomyiasis 
optic nerve disease +   
orbital disease +   
Pancreas Agenesis, Dorsal 
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 +   
thyroid malformation +   
toxocariasis +   
Urinary Tract Abnormalities +   
Urogenital Abnormalities +   
uveal disease +   
Vertebral Fusion Posterior Lumbosacral Blepharoptosis 
Vision Disorders +   
visual pathway disease +   
vitreous detachment +   
vitreous disease +   
 aniridia +   
 Anophthalmia +   
 coloboma +   
 cryptophthalmia +   
 Ectopia Lentis +   
 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.