All diseases

OMIM ID
259770
OMIM term:
OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME; OPPG
Alternative terms:
OPS
OSTEOGENESIS IMPERFECTA, OCULAR FORM
(∗) Location:
11q13.2  
(†) Associated OMIM genes:
LRP5  
(‡) Associated MGI genes:
Lrp5  

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* quick link - http://q.sanger.ac.uk/f73wg4rg