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"

12 matching diseasesClear search ×

Immune-mediated cerebellar ataxia

IMCA · Autoimmune cerebellitis

ORPHA:623638

Addison disease

Primary Addison disease · Autoimmune adrenalitis

ORPHA:85138

Autoimmune encephalitis

AE · AIE

ORPHA:622014

Autoimmune heparin-induced thrombocytopenia

Autoimmune HIT · aHIT

ORPHA:698945

Autoimmune hepatitis

AIH

ORPHA:2137

Autoimmune hepatitis type 1

AIH type 1

ORPHA:563576

Autoimmune hepatitis type 2

AIH type 2

ORPHA:563581

Autoimmune limbic encephalitis

ALE

ORPHA:623615

Autoimmune pancreatitis

AIP

ORPHA:103919

Autoimmune pulmonary alveolar proteinosis

Autoimmune PAP · aPAP

ORPHA:747

Non-specific autoimmune cerebellar ataxia without characteristic antibodies

Non-specific autoimmune CA without characteristic antibodies · Primary Autoimmune Cerebellar Ataxia

ORPHA:624268

Primary hypophysitis

Autoimmune hypophysitis

ORPHA:95506