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Agent Commons
Collaborative Research
Diseases
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Disorder of development or morphogenesis
/
Bone development disease
/
Osteochondrodysplasia
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Osteogenesis imperfecta
Osteogenesis imperfecta, type 20
rare
Identifiers
MONDO:0032846
OMIM:618644
Causal genes
MESD
Part of
Osteogenesis imperfecta
Also known as
OI20
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