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MIM:261630 - HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C
Xenbase Genes: qdpr
Human Disease Resource: MIM
MONDO:0009862 - dihydropteridine reductase deficiency |
MONDO:0016543 - hyperphenylalaninemia due to tetrahydrobiopterin deficiency |
DOID:0081130 - BH4-deficient hyperphenylalaninemia C |