All diseases

OMIM ID
166210
OMIM term:
OSTEOGENESIS IMPERFECTA, TYPE II
Alternative terms:
OI, TYPE II; OI2
OSTEOGENESIS IMPERFECTA CONGENITA, PERINATAL LETHAL FORM
OSTEOGENESIS IMPERFECTA CONGENITA; OIC
VROLIK TYPE OF OSTEOGENESIS IMPERFECTA
(∗) Location:
17q21.33   7q21.3  
(†) Associated OMIM genes:
COL1A1   COL1A2  
(‡) Associated MGI genes:
Col1a1  

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