mild osteogenesis imperfecta Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Osteogenesis imperfecta type I is a mild type of osteogenesis imperfecta (OI; see this term), a genetic disorder characterized by increased bone fragility, low bone mass and susceptibility to bone fractures. (Orphanet Rare Disease Ontology, Orphanet_216796)
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Genes

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

Symbol Name
COL1A1 collagen, type I, alpha 1