Very long chain acyl-CoA dehydrogenase deficiency
ORPHA:26793X-linked agammaglobulinemia
ORPHA:47X-linked creatine transporter deficiency
ORPHA:52503Xanthinuria type I
ORPHA:93601← PrevPage 5 of 5
Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.
Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"
Very long chain acyl-CoA dehydrogenase deficiency
ORPHA:26793X-linked agammaglobulinemia
ORPHA:47X-linked creatine transporter deficiency
ORPHA:52503Xanthinuria type I
ORPHA:93601