Category
page 1Genetic anomalies
Klinefelter's syndrome
human chromosomal condition
chimera
single organism composed of two or more different populations of genetically distinct cells
Prader–Willi syndrome
rare genetic disorder
DiGeorge syndrome
T cell deficiency disease that is the result of a large deletion of chromosome 22, which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production
Smith-Magenis syndrome
Human disease
22q13 deletion syndrome
human disease
chromosome 1p36 deletion syndrome
Human disease
biology of intersex
results of sexual differentiation that are intermediate between male and female poles
Koolen de Vries syndrome
Human disease
chromosome 17q12 deletion syndrome
rare human disease caused by partial deletion of the long arm of chromosome 17