sudden infant death syndrome Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A syndrome that is characterized by the sudden death of an infant that is not predicted by medical history and remains unexplained after a thorough forensic autopsy and detailed death scene investigation. (Human Disease Ontology, DOID_9007)
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
IL10 interleukin 10