Osteogenesis Imperfecta Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D010013
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4 genes/proteins associated with the disease Osteogenesis Imperfecta from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CRTAP cartilage associated protein 2.88009
SPARC secreted protein, acidic, cysteine-rich (osteonectin) 2.88009
P3H1 prolyl 3-hydroxylase 1 2.88009
COL1A1 collagen, type I, alpha 1 2.88009