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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
color blindness +     
achromatopsia +   
A color blindness that is characterized by a congenital cone color vision disorder, the inability to perceive color and to achieve satisfactory visual acuity at high light levels has_material_basis_in autosomal recessive inheritance. (DO)
acquired color blindness 
blue color blindness  
Colorblindness, Partial Tritanomaly 
red color blindness  
red-green color blindness  

Synonyms
Exact Synonyms: ACHM ;   monochromatism
Primary IDs: RDO:9004252
Xrefs: ICD10CM:H53.51 ;   ICD9CM:368.54 ;   NCI:C84528 ;   ORDO:49382
Definition Sources: http://en.wikipedia.org/wiki/Achromatopsia "DO", http://www.ncbi.nlm.nih.gov/books/NBK1418/ "DO", http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=49382 "DO", http://www.sciencedirect.com/science/article/pii/S0161642009010008 "DO"

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