serw-MX  [xml]  
 


    
 DeCS Categories

C10 Nervous System Diseases .
C10.597 Neurologic Manifestations .
C10.597.751 Sensation Disorders .
C10.597.751.941 Vision Disorders .
C10.597.751.941.256 Color Vision Defects .
C11 Eye Diseases .
C11.966 Vision Disorders .
C11.966.256 Color Vision Defects .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.763 Sensation Disorders .
C23.888.592.763.941 Vision Disorders .
C23.888.592.763.941.256 Color Vision Defects .
G10 Digestive System and Oral Physiological Phenomena .
G10.261 Digestive System Physiological Phenomena .
G10.261.165 Defecation .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
/abnormalities .
/agenesis .
/anomalies .
/aplasia .
/atresia .
/birth defects .
/congenital defects .
/defects .
/deformities .
/hypoplasia .
/malformations .
Used with organs for congenital defects producing changes in the morphology of the organ. It is used also for abnormalities in animals. .
1.00
 
Defecation .
Defecations .
The normal process of elimination of fecal material from the RECTUM. .
0.71
1106140
 
Color Vision Defects .
Color Blindness, Acquired .
Color Blindness, Blue .
Color Blindness, Green .
Color Blindness, Inherited .
Color Blindness, Red .
Color Blindness, Red-Green .
Color Vision Deficiency .
Deutan Defect .
Protan Defect .
Tritan Defect .
Acquired Color Blindness .
Blindness, Color .
Blue Color Blindness .
Color Blindness, Red Green .
Color Vision Defect .
Defect, Color Vision .
Defect, Deutan .
Defects, Color Vision .
Green Color Blindness .
Inherited Color Blindness .
Red Color Blindness .
Red-Green Color Blindness .
Vision Defect, Color .
Vision Defects, Color .
Achromatopsia .
Color Blindness .
Monochromatopsia .
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 ROD OPSINS genes (on X CHROMOSOME and CHROMOSOME 3) that code the photopigments for red, green and blue. .
0.68
383431
 
Congenital Abnormalities .
Abnormalities, Congenital .
Defects, Congenital .
Abnormality, Congenital .
Birth Defect .
Congenital Abnormality .
Congenital Defect .
Defect, Birth .
Defect, Congenital .
Defects, Birth .
Deformity .
Congenital Malformations .
Birth Defects .
Deformities .
Congenital Defects .
Abnormalities .
Malformations of organs or body parts during development in utero. .
0.68
199122930