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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
eye disease +     
genetic disease +     
Adrenocortical Hypofunction, Chronic Primary Congenital 
adrenocorticotropic hormone deficiency  
advanced sleep phase syndrome 3  
age related macular degeneration 8  
AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME  
Alagille syndrome  
Aland Island eye disease  
Alpha-2-Deficient Collagen Disease 
amblyopia +   
ancylostomiasis +  
apparent mineralocorticoid excess syndrome  
Aquaporin 1 Deficiency 
aspartylglucosaminuria  
Asthenopia  
ataxic cerebral palsy 
atrial heart septal defect 3  
atrial heart septal defect 4  
autoimmune lymphoproliferative syndrome +   
baylisascariasis 
blindness +   
brachydactyly type A1B 
brachydactyly type A1C  
brachydactyly type A1D  
brachydactyly type B1  
brachydactyly type B2  
brachydactyly type E1  
brachydactyly type E2  
CADASIL +   
CAKUT2  
cataract 23  
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
Cenani-Lenz syndactyly syndrome  
Cerebellar, Ocular, Craniofacial, and Genital Syndrome  
CHARGE syndrome  
chromosomal disease +   
Cogan syndrome +   
complement factor I deficiency  
complex cortical dysplasia with other brain malformations 1  
complex cortical dysplasia with other brain malformations 2  
complex cortical dysplasia with other brain malformations 3  
complex cortical dysplasia with other brain malformations 4  
complex cortical dysplasia with other brain malformations 5  
complex cortical dysplasia with other brain malformations 6  
complex cortical dysplasia with other brain malformations 7  
congenital diarrhea +   
congenital hemolytic anemia +   
Congenital Hepatic Fibrosis  
congenital hypoplastic anemia +   
congenital muscular dystrophy +   
congenital myasthenic syndrome +   
Congenital Pain Insensitivity +   
conjunctival disease +   
corneal disease +   
cysticercosis +  
desquamative interstitial pneumonia  
dipetalonemiasis 
Dwarfism +   
Encephalocraniocutaneous Lipomatosis  
Eye Abnormalities +   
eye accommodation disease +  
eye degenerative disease +   
Eye Hemorrhage +   
Eye Infections +   
Eye Injuries +   
Eye Manifestations +   
Eye Neoplasms +   
eyelid disease +   
Familial Cirrhosis +   
Familial Dysalbuminemic Hyperthyroxinemia  
Familial Hemophagocytic Lymphohistiocytoses +   
familial hypertrophic cardiomyopathy +   
Familial Lipochrome Histiocytosis 
Familial Mixed Cryoglobulinemia  
Familial Temporal Epilepsy +   
frontotemporal dementia and/or amyotrophic lateral sclerosis-3  
frontotemporal dementia and/or amyotrophic lateral sclerosis-4  
fundus dystrophy +   
Genetic Skin Diseases +   
glaucoma +   
globe disease +   
gonorrhea +  
hereditary angioedema +   
Hereditary Bilateral Parotidomegaly 
Hereditary Epistaxis 
Hereditary Eye Diseases +   
Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder.
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
Hereditary Sensorimotor Neuropathy with Upper Motor Neuron, Visual Pathway and Autonomic Disturbance 
Hernandez Fragoso Syndrome 
hypogonadotropic hypogonadism 5 with or without anosmia +   
inherited metabolic disorder +   
Isolated Prolactin Deficiency 
Kallmann syndrome +   
lacrimal apparatus disease +   
Laminopathies  
Lennox-Gastaut syndrome  
lens disease +   
leprosy +   
loiasis 
Marfan syndrome +   
microphthalmia +   
Mollica Pavone Antener Syndrome 
monogenic disease +   
MORM Syndrome  
Nervous System Heredodegenerative Disorders +   
NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES  
NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME  
Neuromuscular Oculoauditory Syndrome  
Nonimmune Chronic Idiopathic Neutropenia, Adult  
ocular albinism +   
ocular hypertension +   
ocular hypotension +   
ocular motility disease +   
Ocular Neovascularization +   
ophthalmia nodosa 
ophthalmomyiasis 
optic nerve disease +   
orbital disease +   
osteochondrodysplasia +   
philophthalmiasis 
polygenic disease +   
primary hypertrophic osteoarthropathy +   
progressive familial intrahepatic cholestasis +   
pulmonary alveolar microlithiasis  
pupil disease +   
refractive error +   
retinal disease +   
Sacral Agenesis with Vertebral Anomalies  
scleral disease +   
scotoma +   
toxocariasis +   
uveal disease +   
Vision Disorders +   
visual pathway disease +   
vitreous detachment +   
vitreous disease +   
yellow nail syndrome +  
 Alacrima +   
 Albinism +   
 aniridia +   
 Choroideremia +   
 gyrate atrophy +   
 megalocornea +   

Synonyms
Exact Synonyms: Hereditary Eye Disease
Primary IDs: MESH:D015785
Alternate IDs: RDO:0001905
Definition Sources: MESH:D015785

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