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"

10 matching diseasesClear search ×

Myasthenia gravis

Acquired myasthenia · Autoimmune myasthenia gravis

ORPHA:589

Acquired arginine vasopressin deficiency

Acquired CDI · Acquired neurogenic diabetes insipidus

ORPHA:95626

Acquired ataxia

ORPHA:247242

Acquired neutropenia

Immunologic neutropenia

ORPHA:178996

Acquired pseudoxanthoma elasticum

Acquired Gronblad-Strandberg-Touraine syndrome · Acquired PXE

ORPHA:228247

Adult-onset myasthenia gravis

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

ORPHA:391490

Immune-mediated thrombotic thrombocytopenic purpura

Acquired thrombotic thrombocytopenic purpura · Acquired TTP

ORPHA:93585

Juvenile myasthenia gravis

Childhood myasthenia gravis · Generalized myasthenia gravis

ORPHA:391497

Rippling muscle disease with myasthenia gravis

Acquired rippling muscle disease · Generalized myasthenia gravis

ORPHA:206575

Transient neonatal myasthenia gravis

Generalized myasthenia gravis · MG

ORPHA:391504