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 ×

OBSOLETE: Isolated optic neuritis without anti-MOG antibodies

OBSOLETE: Isolated optic neuritis without anti-myelin oligodendrocyte glycoprotein antibodies

ORPHA:592885

Acute disseminated encephalomyelitis with anti-MOG antibodies

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

ORPHA:592894

Acute disseminated encephalomyelitis without anti-MOG antibodies

Acute disseminated encephalomyelitis without anti-myelin oligodendrocyte glycoprotein antibodies

ORPHA:592900

Acute transverse myelitis with anti-MOG antibodies

Acute transverse myelitis with anti-myelin oligodendrocyte glycoprotein antibodies

ORPHA:592873

Neuromyelitis optica spectrum disorder with anti-MOG antibodies

Devic disease · Devic syndrome

ORPHA:592856

Neuromyelitis optica spectrum disorder without anti-MOG and without anti-AQP4 antibodies

Devic disease · Devic syndrome

ORPHA:592869

OBSOLETE: Isolated optic neuritis with anti-MOG antibodies

OBSOLETE: Isolated optic neuritis with anti-myelin oligodendrocyte glycoprotein antibodies

ORPHA:592888

Polyneuropathy associated with IgM monoclonal gammopathy with anti-MAG

Anti-MAG neuropathy · Neuropathy associated with monoclonal IgM antibodies to myelin-associated glycoprotein

ORPHA:639