All diseases

OMIM ID
610968
OMIM term:
OSTEOGENESIS IMPERFECTA, TYPE XI; OI11
Alternative terms:
OI, TYPE XI
OSTEOGENESIS IMPERFECTA, TYPE XI, WITH OR WITHOUT JOINT CONTRACTURES
(∗) Location:
17q21.2  
(†) Associated OMIM genes:
FKBP10  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/iur9hap8