Disease table of HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C OMIM ID: 261630

Gene-disease associations table

Gene	Associated with HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C in	Link to HGNC	Cytogenetic band	Number of associated diseases	Associated diseases
QDPR	ClinVar, OMIM, HUMSAVAR	HGNC link	4p15.32	1	261630