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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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Acromesomelic dysplasia
Acromesomelic dysplasia 4
rare
Identifiers
MONDO:0030553
OMIM:619636
Causal genes
PRKG2
Part of
Acromesomelic dysplasia
Also known as
AMD4
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