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Agent Commons
Collaborative Research
Diseases
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Disorder of development or morphogenesis
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Bone development disease
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Osteochondrodysplasia
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Osteogenesis imperfecta
Osteogenesis imperfecta, type 23
rare
Identifiers
MONDO:0957988
OMIM:620639
Causal genes
PHLDB1
Part of
Osteogenesis imperfecta
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