An extra copy of Chromosome 18
Deletion Mutation causes DiGeorges Syndrome.
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.
Down's syndrome is caused by trisomy of the 21st chromosome. This is mostly caused when the chromosome pair fails to separate properly (nondisjunction).
A frameshift mutation in the CARD15 gene
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deletion
Unknown at this time.
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.
It's a gene mutation. And it is different for each organ.
Tourette syndrome is believed to be a complex disorder with a combination of genetic and environmental factors contributing to its development. It is not caused by a single mutation, but rather likely involves several genetic variations that increase susceptibility to the disorder.
that would be a hereditary thing not a gene mutaion
Marfan syndrome is typically caused by mutations in the FBN1 gene, which provides instructions for making a protein called fibrillin-1. These mutations can result in the production of an abnormal fibrillin-1 protein, leading to the characteristic features of Marfan syndrome such as tall stature, long limbs, and cardiovascular issues.