huhuhhuhuhuuh
It's a gene mutation. And it is different for each organ.
There is no single type of mutation that causes Hemophilia A. It is not the type of mutation but rather the location of the mutation within the genetic code.
Deletion Mutation causes DiGeorges Syndrome.
A frameshift mutation in the CARD15 gene
deletion
Unknown at this time.
Bipolar disorder affects men and women equally and usually appears between the ages of 15 and 25. The exact cause is unknown, but it occurs more often in relatives of people with bipolar disorder.
The mutation that causes Autism is a rare genetic mutation. There are three different genes that are linked to the cause of different disorders on the Autism Spectrum.
Noonan syndrome is caused by the mutation in a particular gene. It is a genetic disorder which means that the child which is born with this disorder, must have been in their parents.
Missense
Periodic or cyclic neutropenia is a disorder which causes frequent infections. This condition in which neutrophils, a type of white blood cell, decrease on a regular basis is extremely rare and has been shown to be a genetic mutation.
that would be a hereditary thing not a gene mutaion