legg-perthes disease Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Avascular necrosis of the proximal epiphysis of the femur occurring in growing children and caused by an interruption of the blood supply to the head of the femur close to the hip joint. The necrosis is characteristically associated with flattening of the femoral head, for which reason the term coxa plana has been used to refer to this feature in the medical literature. (Human Phenotype Ontology, HP_0005743)
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Genes

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

Symbol Name
FGB fibrinogen beta chain