Disease-gene associations mined from literature

Human genes for cryptorchidism

Cryptorchidism [DOID:11383]

Cryptorchidism is the absence of one or both testes from the scrotum. It is the most common birth defect regarding male genitalia. In unique cases, cryptorchidism can develop later in life, often as late as young adulthood. About 3% of full-term and 30% of premature infant boys are born with at least one undescended testis. However, about 80% of cryptorchid testes descend by the first year of life (the majority within three months), making the true incidence of cryptorchidism around 1% overall. Cryptorchidism is distinct from monorchism the condition of having only one testicle.

Synonyms:  cryptorchidism,  DOID:11383,  Cryptorchidism NOS (disorder),  Cryptorchism,  Cryptorchism (disorder) ...

Linkouts:  OMIM