Additional Disease Briefs

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Use the form below to explore NORD's comprehensive rare disease database. Search for detailed information on rare diseases, including NORD's authoritative Rare Disease Reports and data from other reliable sources.
* = NORD Rare Disease Report

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Rare Disease Database Reports Additional Rare Disease Briefs
osteoblastoma

Also known as: giant osteoid osteoma, ossifying giant cell tumor, ossifying giant cell tumour, osteoblastoma, osteoblastoma (disease), osteoblastoma, benign

osteochondrosis

Also known as: apophysitis, epiphyseal necrosis, epiphysitis, osteochondritis, osteochondritis juvenilis, osteochondrosis not specified as adult or juvenile, of unspecified site

osteocraniostenosis

Also known as: GCLEB, Habrodysplasia, Osteocraniosplenic syndrome, gracile bone dysplasia, osteocraniostenosis, skeletal dysplasia lethal with gracile bones, skeletal dysplasia, lethal, with gracile bones

osteofibrous dysplasia

Also known as: Kempson-Campanacci lesion, OFD, OSFD, cortical fibrous dysplasia, ossifying fibroma of long bones, osteofibrous dysplasia, osteofibrous dysplasia of bone, osteofibrous dysplasia, susceptibility to, tibia, bowing of, with pseudarthrosis and pectus excavatum

osteogenesis imperfecta type 1

Also known as: Adair-Dighton syndrome, OI type 1, OI, type 1, OI1, Van der Hoeve syndrome, classic non-deforming OI with blue sclerae, mild osteogenesis imperfecta, non-deforming osteogenesis imperfecta, osteogenesis imperfecta tarda, osteogenesis imperfecta type 1, osteogenesis imperfecta type I, osteogenesis imperfecta with blue sclerae, osteogenesis imperfecta, type 1, osteogenesis imperfecta, type I

osteogenesis imperfecta type 10

Also known as: OI type 10, OI type X, OI, type 10, OI10, SERPINH1 osteogenesis imperfecta, osteogenesis imperfecta caused by mutation in SERPINH1, osteogenesis imperfecta type X, osteogenesis imperfecta, type 10, osteogenesis imperfecta, type X

osteogenesis imperfecta type 11

Also known as: FKBP10 osteogenesis imperfecta, OI type 11, OI type XI, OI, type 11, OI11, osteogenesis imperfecta caused by mutation in FKBP10, osteogenesis imperfecta type XI, osteogenesis imperfecta, type 11, osteogenesis imperfecta, type XI

osteogenesis imperfecta type 12

Also known as: OI, type 12, OI12, SP7 osteogenesis imperfecta, osteogenesis imperfecta caused by mutation in SP7, osteogenesis imperfecta type XII, osteogenesis imperfecta, type 12, osteogenesis imperfecta, type XII

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  12. 1032