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"

9 matching diseasesClear search ×

NMDA receptor encephalitis

Limbic encephalitis with NMDA receptor antibodies · Limbic encephalitis with N-methyl-D-aspartate receptor antibodies

ORPHA:217253

Acute disseminated encephalomyelitis with anti-MOG antibodies

ADEM with anti-MOG antibodies · Acute disseminated encephalomyelitis with anti-myelin oligodendrocyte glycoprotein antibodies

ORPHA:592894

Autoimmune limbic encephalitis

ALE

ORPHA:623615

OBSOLETE: Limbic encephalitis associated with antibodies to cell membrane antigens

ORPHA:163903

OBSOLETE: Limbic encephalitis with caspr2 antibodies

ORPHA:276402

OBSOLETE: Limbic encephalitis with DPP6 antibodies

OBSOLETE: Limbic encephalitis with dipeptidyl-peptidase 6 antibodies · OBSOLETE: Limbic encephalitis with DPPX antibodies

ORPHA:329341

OBSOLETE: Limbic encephalitis with LGI1 antibodies

OBSOLETE: Limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies

ORPHA:163908

OBSOLETE: Limbic encephalitis with nCMAgs antibodies

OBSOLETE: Limbic encephalitis with novel cell membrane antigen antibodies

ORPHA:163914

OBSOLETE: Limbic encephalitis with neurexin-3 antibodies

ORPHA:498700