All diseases

OMIM ID
166200
OMIM term:
OSTEOGENESIS IMPERFECTA, TYPE I
Alternative terms:
OI, TYPE I; OI1
OSTEOGENESIS IMPERFECTA TARDA
OSTEOGENESIS IMPERFECTA WITH BLUE SCLERAE OSTEOPENIC NONFRACTURE SYNDROME, INCLUDED
(∗) Location:
17q21.33  
(†) Associated OMIM genes:
COL1A1  
(‡) Associated MGI genes:
Col1a1  

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