Color Blindness:
Color blindness is a genetic condition affecting color perception.
Genes for color vision are located on the X chromosome.
Normal vision (XNXN), carrier (XNXn), and color blind (XnY) genotypes.
Carriers are typically females with one normal and one mutated allele.
Color blindness is more common in males.
Prenatal diagnosis is possible.
Welcome to SATHEE !
Select from 'Menu' to explore our services, or ask SATHEE to get started. Let's embark on this journey of growth together! 🌐📚🚀🎓
I'm relatively new and can sometimes make mistakes.
If you notice any error, such as an incorrect solution, please use the thumbs down icon to aid my learning.
To begin your journey now, click on "I understand".
