DISEASES

Disease-gene associations mined from literature

Human genes for osteogenesis imperfecta

Osteogenesis imperfecta [DOID:12347]

An osteochondrodysplasia that has_material_basis_in a deficiency in type-I collagen which results_in brittle bones and defective connective tissue.

Synonyms:  osteogenesis imperfecta,  DOID:12347,  Lobstein's syndrome,  Osteopsathyrosis,  Vrolik's disease ...

Linkouts:  OMIM #1 #2 #3 #4 #5 #6 #7 #8 #9 #10 #11 #12 #13 #14 #15 #16 #17 #18