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, osteogenesis imperfectas, brittle bone disease, Lobstein's syndrome ...
Linkouts: OMIM #1 #2 #3 #4 #5 #6 #7 #8 #9 #10 #11 #12 #13 #14 #15 #16 #17 #18