Question

Haemophilia is
(a) autosomal (b) Y-linked
(c) Z-linked (d) X-linked

Answer 1

Answer:

I hope the answer is autosomal

Answer 2

Hemophilia is a X linked recessive pattern of genetic disease

Explanation:

Hemophilia is a genetic disorder which is mainly caused by genes that are located on the X linked chromosome. The affected person looses it's ability to  make blood clot and as a result, bleeding occur for a longer time.

Hemophilia are of 2 types- Hemophilia A and Hemophilia B.

Hemophilia A mainly occur due low amount of blood clotting factor VIII and Hemophilia B is mainly caused by low level of blood clotting factor IX.

Another type of Hemophilia is seen called as Hemophilia C that is mainly cause due to low level of blood clotting factor XI.

The complications that the affected persons are faced-deep internal bleeding,joint damage,intracranial hemorrhage.