LHX9
Description
The LHX9 (LIM homeobox 9) is a protein-coding gene located on chromosome 1.
Plays a crucial role in the development of the gonads, the reproductive organs.
LHX9 is also known as -.
Associated Diseases
- pituitary stalk interruption syndrome
- isolated congenital hypogonadotropic hypogonadism
- 46,XY partial gonadal dysgenesis
- 46,XX testicular disorder of sex development
- 46,XY complete gonadal dysgenesis
- Kallmann syndrome
- partial androgen insensitivity syndrome
- 46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome
