An abnormal number of chromosomes is called aneuploidy. If a chromosome has 3 of its kind, it is trisomic. The exact condition depends on which gene has the extra chromosome.
Xi or just X depending on how you want to write it
There is no 'deletion chromosome'. You mean chromosome deletion, and it is a phenomenon where a chromosome disappears from cell's genetic layout.
Hypertrichosis can have various underlying genetic causes. Specific genes that have been associated with hypertrichosis include the SOX3 gene on the X chromosome and the FOXC2 gene on chromosome 16. However, hypertrichosis can also be a symptom of other genetic or chromosomal abnormalities.
The X chromosome contains considerably more genetic material than the Y chromosome.
nucleus → chromosome → gene
This would be just a genetic or inherited condition.
This would be just a genetic or inherited condition.
Klinefelter syndrome is a genetic condition that results when a boy is born with an extra copy of the X chromosome. Klinefelter syndrome is a common genetic condition affecting males.
The most common condition associated with a deletion of the end of chromosome 5 is: cri-du-chat syndrome.
This would be just a genetic or inherited condition.
The DNA molecules in various combinations form the genes which are the genetic code of a chromosome.
Xi or just X depending on how you want to write it
There is no 'deletion chromosome'. You mean chromosome deletion, and it is a phenomenon where a chromosome disappears from cell's genetic layout.
Genetic :-)
There is no such condition as Wolfhousen Syndrome. Assuming that you mean Wolf-Hirschhorn Syndrome, this is a condition that arises due to a genetic error in chromosome 4 and affects various parts of the body.
A genetic condition caused by the absence of chromosomal material from chromosome 15. Characteristics include developmental delay, unique physical features and insatiable appetite.
Hypertrichosis can have various underlying genetic causes. Specific genes that have been associated with hypertrichosis include the SOX3 gene on the X chromosome and the FOXC2 gene on chromosome 16. However, hypertrichosis can also be a symptom of other genetic or chromosomal abnormalities.