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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
/
Hereditary disease
/
Skeletal dysplasia
/
Acromelic dysplasia
Peripheral dysostosis
rare
Identifiers
MONDO:0008227
OMIM:170700
Orphanet:1795
Part of
Acromelic dysplasia
Also known as
dysostosis peripheral
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