All diseases

OMIM ID
166220
OMIM term:
OSTEOGENESIS IMPERFECTA, TYPE IV
Alternative terms:
OI, TYPE IV
OI4
OSTEOGENESIS IMPERFECTA WITH NORMAL SCLERAE
(∗) Location:
17q21.33   7q21.3  
(†) Associated OMIM genes:
COL1A1   COL1A2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/5vi3zvoh