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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 1  
advanced sleep phase syndrome 2  
advanced sleep phase syndrome 3  
age related macular degeneration 8  
Alagille syndrome  
Aland Island eye disease  
Alpha-2-Deficient Collagen Disease 
Alzheimer's disease 18  
amblyopia +   
ancylostomiasis +  
Aquaporin 1 Deficiency  
asthenopia  
ataxia telangiectasia +   
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 1 multiple types  
cataract 10 multiple types  
cataract 11 multiple types +   
cataract 12 multiple types  
cataract 13 with adult i phenotype  
cataract 14 multiple types  
cataract 15 multiple types  
cataract 16 multiple types  
cataract 18  
cataract 2 multiple types  
cataract 20 multiple types  
cataract 21 multiple types  
cataract 23  
cataract 24 
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
cataract 29 
cataract 3 multiple types  
cataract 30  
cataract 31 multiple types  
cataract 33  
cataract 36  
cataract 37 
cataract 38  
cataract 41  
cataract 42  
cataract 43  
cataract 44  
cataract 45  
cataract 46 juvenile-onset  
Cataract 48  
cataract 5 multiple types  
cataract 7  
cataract 8 multiple types 
cataract 9 multiple types  
Cenani-Lenz syndactyly syndrome  
CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME  
CHARGE syndrome  
cherubism +   
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 +   
FTDALS3  
FTDALS4  
fundus dystrophy +   
Genetic Skin Diseases +   
glaucoma +   
globe disease +   
gonorrhea +  
hereditary angioedema +   
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 
hyperimmunoglobulin syndrome +   
hypogonadotropic hypogonadism 5 with or without anosmia +   
IMMUNODEFICIENCY 31B  
Immunodeficiency 38, with Basal Ganglia Calcification  
inherited blood coagulation disease +   
inherited metabolic disorder +   
Isolated Prolactin Deficiency 
Kallmann syndrome +   
Kartagener syndrome  
lacrimal apparatus disease +   
Laminopathies  
Lennox-Gastaut syndrome  
lens disease +   
leprosy +   
loiasis 
Marfan syndrome +   
microphthalmia +   
Mollica Pavone Antener Syndrome 
MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY  
monogenic disease +   
MORM Syndrome  
Nervous System Heredodegenerative Disorders +   
NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES  
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 +   
Parotidomegaly, Hereditary Bilateral 
philophthalmiasis 
platelet-type bleeding disorder 10  
polycystic kidney disease +   
polygenic disease +   
primary hypertrophic osteoarthropathy +   
progressive familial intrahepatic cholestasis +   
pulmonary alveolar microlithiasis  
pupil disease +   
RASopathies  
refractive error +   
retinal disease +   
Rh deficiency syndrome  
Sacral Agenesis with Vertebral Anomalies  
scleral disease +   
scotoma +  
toxocariasis +   
uveal disease +   
Vision Disorders +   
visual pathway disease +   
vitreous detachment +   
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.