• Thumbnail for Osteoporosis-pseudoglioma syndrome
    Osteoporosis-pseudoglioma syndrome or OPGG is a rare genetic condition characterized by early-onset blindness and severe osteoporosis alongside seemingly...
    10 KB (818 words) - 16:38, 20 July 2024
  • Osteopoikilosis Osteoporosis macrocephaly mental retardation blindness Osteoporosis oculocutaneous hypopigmentation syndrome Osteoporosis pseudoglioma syndrome Osteoporosis...
    10 KB (818 words) - 01:37, 27 October 2023
  • Thumbnail for LRP5
    changes in bone mass. A loss-of-function mutation causes osteoporosis pseudoglioma syndrome with a decrease in bone mass, while a gain-of-function mutation...
    24 KB (3,205 words) - 21:15, 27 March 2024
  • Thumbnail for Bone density
    for osteoporosis risk and to identify those who might benefit from measures to improve bone strength. A bone density test may detect osteoporosis or osteopenia...
    18 KB (1,936 words) - 16:33, 20 July 2024
  • Syndromic microphthalmia is a class of rare congenital anomalies characterized by microphthalmia along with other non-ocular malformations. Syndromic...
    13 KB (538 words) - 09:46, 18 March 2024
  • Pedro Pan Opponents Points per game, in sports statistics Osteoporosis-pseudoglioma syndrome, a medical condition This disambiguation page lists articles...
    497 bytes (87 words) - 12:08, 13 September 2022
  • neurological anomalies. Osteoporosis-pseudoglioma syndrome, genetic disorder which combines the association of osteoporosis and pseudoglioma. Osteogenesis imperfecta...
    10 KB (1,081 words) - 15:15, 27 October 2023
  • which contribute to osteoporosis. Loss of function mutations in LRP5 have been implicated in Osteoporosis-pseudoglioma syndrome, Familial exudative vitreoretinopathy...
    21 KB (3,129 words) - 10:03, 2 June 2024
  • TCIRG1 Osteopoikilosis; 166700; LEMD3 Osteoporosis, involutional; 166710; VDR Osteoporosis-pseudoglioma syndrome; 259770; LRP5 Osteosarcoma; 259500; LOH18CR1...
    234 KB (18,877 words) - 15:43, 9 May 2024