Additional Disease Briefs

osteopetrosis, autosomal dominant 3

Also known as: OPTA3, OSTEOPETROSIS, autosomal dominant 3

osteoporosis-pseudoglioma syndrome

Also known as: OPPG, Ops, ocular form of osteogenesis imperfecta, osteogenesis imperfecta ocular form, osteogenesis imperfecta, ocular form, osteoporosis pseudoglioma syndrome, osteoporosis-pseudoglioma syndrome, pseudoglioma with bone fragility

osteoradionecrosis of the mandible

osteosclerosis-developmental delay-craniosynostosis syndrome

osteosclerotic metaphyseal dysplasia

Also known as: OSMD, osteosclerotic metaphyseal dysplasia

otodental syndrome

Also known as: chromosome 11q13 deletion syndrome, globodontia, oculootodental syndrome, otodental dysplasia, otodental dysplasia chromosome deletion syndrome, otodental syndrome, otodental syndrome with coloboma

otofaciocervical syndrome

Also known as: Fara Chlupackova syndrome, Fara-Chlupackova syndrome, OFC syndrome, familial oto-facio-cervical dysmorphia

otofaciocervical syndrome 1

Also known as: EYA1 otofaciocervical syndrome, OFC, OFC1, OTFCS, otofaciocervical syndrome, otofaciocervical syndrome 1, otofaciocervical syndrome caused by mutation in EYA1

otofaciocervical syndrome 2

Also known as: OFC2, OTFCS2, PAX1 otofaciocervical syndrome, otofaciocervical syndrome 2, otofaciocervical syndrome caused by mutation in PAX1, otofaciocervical syndrome type 2