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"

3 matching diseasesClear search ×

Secondary neonatal autoimmune disease

Transplacentally acquired neonatal autoimmune disease

ORPHA:398091

Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization

Alloimmune neonatal renal disease · FMAIG

ORPHA:69063

Transient neonatal myasthenia gravis

Generalized myasthenia gravis · MG

ORPHA:391504