deletion
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.
The specific location of the mutation that causes X-ALD is on the ABCD1 gene on the X-chromosome. Please note that there isn't a specific mutation in the ABCD1 gene that causes X-ALD or can be related in any way to the different clinical presentations of the disease.
Adrenoleukodystrophy (ALD) is primarily caused by a mutation in the ABCD1 gene, which encodes a protein involved in the transport of very long-chain fatty acids (VLCFAs) into peroxisomes. This mutation typically results in a loss of function of the ABCD1 protein, leading to the accumulation of VLCFAs in the body. The genetic mutation is inherited in an X-linked recessive manner, meaning it predominantly affects males, while female carriers may exhibit milder symptoms.
A frameshift mutation in the CARD15 gene
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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.
that would be a hereditary thing not a gene mutaion
The United Leukodystrophy Foundation (see related links) mentions an x-linked adrenoleukodystrophy, as well as other adrenoleukodystrophies that have multiple possible genetic causes.
This disease results from a mutation on the x-chromosome. It's recessive considering that a dominant will only cover up things that have occur, for example the damage that has occured, with something else. A recessive will continue to give latent traits. The allele in Adrenoleukodystrophy can only be caused by heredity mutation thus making it recessive.