The way property values are displayed:
The way concept relations are shown:
The way concept relations are shown:
Color Vision Defects
Hierarchy: | ∟ ∟ ∟ Color Vision Defects 8 coordinate concepts∟ ∟ ∟ ∟ ∟ Color Vision Defects 8 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ Color Vision Defects 8 coordinate conceptsX |
Broader terms: | |
historyNote*: | 90; was COLOR BLINDNESS 1963-89
X |
onlineNote*: | use COLOR VISION DEFECTS to search COLOR BLINDNESS 1966-89
X |
publicMeSHNote*: | 90; was COLOR BLINDNESS 1963-89
X |
Scope note: | Defects 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 OPSIN genes (on X CHROMOSOME and CHROMOSOME 3) that code the photopigments for red, green and blue.
X |
activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateRevised*: | 2005-07-12X |
recordAuthorizer*: | agsX |
recordMaintainer*: | agsX |
recordOriginator*: | NLMX |
Related term: | |
Type: | |
Coordinate terms: | |
URI: | |
Labels and equivalent concepts: | Värinäön häiriöt (fi) XVärinäön häiriö (fi, replaced) Värinäön poikkeama (fi, replaced) Värisokeus (fi, replaced) Värinäkövika (fi, replaced) Värinäköhäiriöt (fi, replaced) Poikkeava värinäkö (fi, replaced) Värinäköhäiriö (fi, replaced) Färgblindhet (sv) Protan Defect (en, replaced) Tritan Defect (en, replaced) Deutan Defect (en, replaced) Defectus visus colorum (la-FI, replaced) |
Share: |
Loading results...