15 relations: Klinefelter syndrome, Sex chromosome, Tetrasomy X, Triple X syndrome, Turner syndrome, XX gonadal dysgenesis, XX male syndrome, XXXY syndrome, XXYY syndrome, XY gonadal dysgenesis, XYY syndrome, 45,X/46,XY mosaicism, 46, XX/46,XY, 49,XXXXX, 49,XXXXY.
Klinefelter syndrome (KS) also known as 47,XXY or XXY, is the set of symptoms that result from two or more X chromosomes in males.
An allosome (also referred to as a sex chromosome, heterotypical chromosome, heterochromosome, or idiochromosome) is a chromosome that differs from an ordinary autosome in form, size, and behavior.
Tetrasomy X (also called XXXX syndrome, quadruple X, or 48,XXXX) is an extremely rare chromosomal disorder caused by the presence of four X chromosomes instead of two X chromosomes.
Triple X syndrome, also known as trisomy X and 47,XXX, is characterized by the presence of an extra X chromosome in each cell of a female.
Turner syndrome (TS), also known as 45,X or 45,X0, is a condition in which a female is partly or completely missing an X chromosome.
This syndrome is inherited as an autosomal disease.
XX male syndrome is a rare congenital condition where an individual with a female genotype has phenotypically male characteristics that can vary between cases.
XXXY syndrome is a genetic disorder characterized by a sex chromosome aneuploidy, where males have two extra X chromosomes.
XXYY syndrome is a sex chromosome anomaly in which males have an extra X and Y chromosome.
Swyer syndrome, or XY gonadal dysgenesis, is a type of hypogonadism in a person whose karyotype is 46,XY.
XYY syndrome is a genetic condition in which a male has an extra Y chromosome.
45,X/46,XY mosaicism, also known as X0/XY mosaicism and mixed gonadal dysgenesis, "45,X/46,XY including Y chromosome rearrangements".
46,XX/46,XY is a chimeric genetic disorder caused by having two distinct cell populations within the body.
49,XXXXX, also known as pentasomy X, is a chromosome abnormality where a female has five X chromosomes rather than the normal two.
49,XXXXY syndrome is an extremely rare aneuploidic sex chromosomal abnormality.