Disease table of HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A OMIM ID: 261640

Gene-disease associations table

GeneAssociated with HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
PTSClinVar, OMIM, HUMSAVARHGNC link11q23.11261640

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