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created at 2021-12-22 03:08:20 UTC
updated at 2021-12-22 07:06:09 UTC
MONDO_bioport_pref_name
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Id
ARTHROGRYPOSIS multiplex congenita, neurogenic, with myelin defect; AMCNMY http://purl.obolibrary.org/obo/MONDO_0060486
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