Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
lens disease +     
monogenic disease +     
Alport syndrome +   
amyotrophic lateral sclerosis +   
Aphakia +   
Artificial Lens Implant Migration 
autosomal genetic disease +   
Bartter disease +   
basal laminar drusen  
Brugada syndrome 2  
Brugada syndrome 3  
Brugada syndrome 4  
Brugada syndrome 5  
Brugada syndrome 6  
Brugada syndrome 8  
Camurati-Engelmann disease +   
cardiofaciocutaneous syndrome +   
cataract +   
Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, location) or etiology (cause and time of occurrence). (Dorland, 27th ed)
catecholaminergic polymorphic ventricular tachycardia +   
Cayman type cerebellar ataxia  
Charcot-Marie-Tooth disease +   
cone-rod dystrophy +   
lens subluxation +   
Opitz-GBBB syndrome +   
X-linked monogenic disease +   
Y-linked monogenic disease +   
 senile cataract +   

Synonyms
Exact Synonyms: Cataracts ;   Lens Opacification ;   Lens Opacities ;   Lens Opacity ;   Membranous Cataract ;   Membranous Cataracts ;   Pseudoaphakia ;   Pseudoaphakias
Narrow Synonyms: CONGENITAL NUCLEAR CATARACT ;   CORTICAL PULVERULENT CATARACT ;   Cataract, Congenital
Primary IDs: MESH:D002386
Alternate IDs: RDO:0000251
Xrefs: OMIM:PS116200
Definition Sources: MESH:D002386, http://en.wikipedia.org/wiki/Cataract, http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001996/, https://www.ncbi.nlm.nih.gov/pubmed/10414631

paths to the root

NHLBI Logo

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