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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
183,974 entries

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Label
Id
genetic defect in, 3 thyroid hormonogenesis C562769
congenital, due to dyshormonogenesis, 3 hypothyroidism C562769
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