osteogenesis imperfecta type 4 https://github.com/monarch-initiative/mondo/issues/4948 https://www.malacards.org/card/osteogenesis_imperfecta_type_iv GARD:0008696 MEDGEN:78665 Orphanet:216820 icd11.foundation:829297901 OI type 4 osteogenesis imperfecta, type IV OI4 SCTID:205497004 MESH:C536045 NCIT:C98576 DOID:0110340 MONDO:0008148 common variable OI with normal sclerae OI type IV osteogenesis imperfecta type IV Osteogenesis imperfecta type IV is a moderate type of osteogenesis imperfecta (OI), a genetic disorder characterized by increased bone fragility, low bone mass and susceptibility to bone fractures. Patients with type IV have moderately short stature, mild to moderate scoliosis, grayish or white sclera, and dentinogenesis imperfecta (DI). osteogenesis imperfecta with normal sclerae OMIM:166220 OI, type 4 osteogenesis imperfecta, type 4 UMLS:C0268363 osteogenesis imperfecta and a reduction of bone mineral density.