CGB2
Description
The CGB2 (chorionic gonadotropin subunit beta 2) is a protein-coding gene located on chromosome 19.
CGB2 may refer to:
CGB2 is also known as -.
Associated Diseases
- Kallmann syndrome
- isolated congenital hypogonadotropic hypogonadism
- hypogonadotropic hypogonadism
- 46,XX testicular disorder of sex development
- partial androgen insensitivity syndrome
- 46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome
- male infertility with teratozoospermia due to single gene mutation
- 46,XY complete gonadal dysgenesis
- 46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency
- partial chromosome Y deletion
- congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency
- 46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency
- ring chromosome Y
- hypogonadotropic hypogonadism 23 with or without anosmia
- obesity due to congenital leptin deficiency
- isochromosomy Yp
- primary hypergonadotropic hypogonadism-partial alopecia syndrome