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
| 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 |
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C130998
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