osteoporosis-pseudoglioma syndrome (Q32136402)

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Osteoporosis pseudoglioma syndrome is a very rare autosomal recessive disorder characterized by congenital or infancy-onset blindness and severe juvenile-onset osteoporosis and spontaneous fractures
  • OPPG
  • ocular form of osteogenesis imperfecta
  • Osteogenesis Imperfecta, Ocular Form
  • Ops
  • OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME
  • OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME; OPPG
  • Osteogenesis imperfecta ocular form
  • Osteoporosis pseudoglioma syndrome
  • Pseudoglioma with bone fragility
  • Osteoporosis-pseudoglioma syndrome
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Language Label Description Also known as
English
osteoporosis-pseudoglioma syndrome
Osteoporosis pseudoglioma syndrome is a very rare autosomal recessive disorder characterized by congenital or infancy-onset blindness and severe juvenile-onset osteoporosis and spontaneous fractures
  • OPPG
  • ocular form of osteogenesis imperfecta
  • Osteogenesis Imperfecta, Ocular Form
  • Ops
  • OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME
  • OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME; OPPG
  • Osteogenesis imperfecta ocular form
  • Osteoporosis pseudoglioma syndrome
  • Pseudoglioma with bone fragility
  • Osteoporosis-pseudoglioma syndrome

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