X-linked recessive is the type of inheritance pattern that hemophilia and color blindness show.
Hemophilia is a sex linked gene carried in the x chromosome.
Yes, hemophilia is sex-linked.
Hemophilia is broken into three subcategories; Hemophilia A, Hemophilia B, and Hemophilia C. These subcategories designate a person as having a deficiency of one of three specific clotting proteins. Hemophilia A is the deficiency of the protein called Clotting Factor VIII. Hemophilia B is the deficiency of Clotting Factor IX. Hemophilia C is the deficiency of Clotting Factor XI. "Royal" hemophilia is simply a reference to Hemophilia B and is therefore a result of a deficiency in the Clotting Factor IX protein. It is sometimes called the royal disease because it has been known to have been passed through some royal families throughout history.
X-Linked Inheritance
Gregor Johann Mendel is credited with discovering the pattern of genetic inheritance
Royal Hemophilia is a reference to Hemophilia B, also known as Factor IX (9) deficiency. This is a genetic disorder that can be inherited. Also near 30% of the Hemophilia B cases result from spontaneous mutations and are not inherited at all. That being said, once the mutation has occurred, that individual can pass the mutation on.
Types of dominance, multiple alleles, sex linked inheritance, polygenic inheritance and maternal inheritance.
pedigree
Pedigree
Polygenic inheritance
Polygenic trait
Multiple gene inheritance. Sree