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MIM:261640 - HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A
Xenbase Genes: pts
Human Disease Resource: MIM
MONDO:0009863 - BH4-deficient hyperphenylalaninemia A |
MONDO:0016543 - hyperphenylalaninemia due to tetrahydrobiopterin deficiency |
DOID:0090106 - BH4-deficient hyperphenylalaninemia A |