|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An osteochondrodysplasia that has_material_basis_in a deficiency in type-I collagen which results_in brittle bones and defective connective tissue. (Human Disease Ontology, DOID_12347)|
|Downloads & Tools|
4 genes/proteins associated with the disease Osteogenesis Imperfecta from the curated CTD Gene-Disease Associations dataset.