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2010 MeSH

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Color Vision Defects
MeSH HeadingColor Vision Defects
Tree NumberC10.597.751.941.256
Tree NumberC11.966.256
Tree NumberC23.888.592.763.941.256
Scope NoteDefects of color vision are mainly hereditary traits but can be secondary to acquired or developmental abnormalities in the CONES (RETINA). Severity of hereditary defects of color vision depends on the degree of mutation of the ROD OPSINS genes (on X CHROMOSOME and CHROMOSOME 3) that code the photopigments for red, green and blue.
Entry TermAchromatopsia
Entry TermColor Blindness
Entry TermColor Blindness, Acquired
Entry TermColor Blindness, Blue
Entry TermColor Blindness, Green
Entry TermColor Blindness, Inherited
Entry TermColor Blindness, Red
Entry TermColor Blindness, Red-Green
Entry TermDeutan Defect
Entry TermMonochromatopsia
Entry TermProtan Defect
Entry TermTritan Defect
See AlsoRetinal Cone Photoreceptor Cells
See AlsoRetinal Diseases
Allowable QualifiersBL CF CI CL CN CO DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RA RH RI RT SU TH UR US VE VI
Online Noteuse COLOR VISION DEFECTS to search COLOR BLINDNESS 1966-89
History Note90; was COLOR BLINDNESS 1963-89
Date of Entry19990101
Unique IDD003117


MeSH Tree Structures

 
Nervous System Diseases [C10]
   Neurologic Manifestations [C10.597]
      Sensation Disorders [C10.597.751]
         Vision Disorders [C10.597.751.941]
Amblyopia [C10.597.751.941.073]
Blindness [C10.597.751.941.162]  +
Color Vision Defects [C10.597.751.941.256]
Diplopia [C10.597.751.941.339]
Hemianopsia [C10.597.751.941.512]
Photophobia [C10.597.751.941.661]
Scotoma [C10.597.751.941.811]
Vision, Low [C10.597.751.941.905]

 
Eye Diseases [C11]
   Vision Disorders [C11.966]
Amblyopia [C11.966.073]
Blindness [C11.966.075]  +
Color Vision Defects [C11.966.256]
Diplopia [C11.966.339]
Night Blindness [C11.966.671]
Photophobia [C11.966.741]
Scotoma [C11.966.811]
Susac Syndrome [C11.966.858]
Vision, Low [C11.966.905]

 
Pathological Conditions, Signs and Symptoms [C23]
   Signs and Symptoms [C23.888]
      Neurologic Manifestations [C23.888.592]
         Sensation Disorders [C23.888.592.763]
            Vision Disorders [C23.888.592.763.941]
Amblyopia [C23.888.592.763.941.073]
Blindness [C23.888.592.763.941.162]  +
Color Vision Defects [C23.888.592.763.941.256]
Diplopia [C23.888.592.763.941.339]
Hemianopsia [C23.888.592.763.941.512]
Photophobia [C23.888.592.763.941.661]
Scotoma [C23.888.592.763.941.811]
Vision, Low [C23.888.592.763.941.848]

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