Rare Disease Library

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"

4 matching diseasesClear search ×

Transient tyrosinemia of the newborn

Transient tyrosinemia of the neonate

ORPHA:3402

Transient familial neonatal hyperbilirubinemia

Lucey-Driscoll syndrome

ORPHA:2312

Transient hyperammonemia of the newborn

ORPHA:289877

Transient neonatal multiple acyl-CoA dehydrogenase deficiency

Transient neonatal MAD deficiency · Transient neonatal MADD

ORPHA:329942