Any osteogenesis imperfecta in which the cause of the disease is a variant in the COL1A2 gene.
Comprehensive, easy-to-understand information about this condition
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brittle bone disorder
MONDO:0011375
osteogenesis imperfecta type 13
MONDO:0013924
osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome
MONDO:0017196
high bone mass osteogenesis imperfecta
MONDO:0017791
osteogenesis imperfecta, IIA 22
MONDO:0030714
osteogenesis imperfecta, type 21
MONDO:0030861