All diseases

OMIM ID
610682
OMIM term:
OSTEOGENESIS IMPERFECTA, TYPE VII
Alternative terms:
OI, TYPE VII
OI7
OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY
(∗) Location:
3p22.3  
(†) Associated OMIM genes:
CRTAP  
(‡) Associated MGI genes:
Crtap  

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* quick link - http://q.sanger.ac.uk/pp23c61l