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"

8 matching diseasesClear search ×

Transient neonatal myasthenia gravis

Generalized myasthenia gravis · MG

ORPHA:391504

Adult-onset myasthenia gravis

Adult-onset acquired myasthenia · Adult-onset autoimmune myasthenia gravis

ORPHA:391490

Juvenile myasthenia gravis

Childhood myasthenia gravis · Generalized myasthenia gravis

ORPHA:391497

Myasthenia gravis

Acquired myasthenia · Autoimmune myasthenia gravis

ORPHA:589

Secondary neonatal autoimmune disease

Transplacentally acquired neonatal autoimmune disease

ORPHA:398091

Transient erythroblastopenia of childhood

Transient acquired pure red cell aplasia

ORPHA:98871

Transient neonatal diabetes mellitus

TNDM

ORPHA:99886

Transient neonatal multiple acyl-CoA dehydrogenase deficiency

Transient neonatal MAD deficiency · Transient neonatal MADD

ORPHA:329942