cryptorchidism. Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Cryptorchidism (derived from the Greek κρυπτός, kryptos, meaning hidden and ὄρχις, orchis, meaning testicle) 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. (Experimental Factor Ontology, EFO_0004562)
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Genes

1 genes associated with the disease cryptorchidism. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
INSL3 insulin-like 3 (Leydig cell)