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MIM:617384 - HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT; HPANBH4
Xenbase Genes: dnajc12
Human Disease Resource: MIM
MONDO:0044304 - hyperphenylalaninemia due to DNAJC12 deficiency |
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MONDO:0044304 - hyperphenylalaninemia due to DNAJC12 deficiency |