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"

7 matching diseasesClear search ×

Polyneuropathy associated with IgM monoclonal gammopathy with anti-MAG

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

ORPHA:639

Acute macular neuroretinopathy

AMNR

ORPHA:488239

Acute motor axonal neuropathy

AMAN · Acute pure motor GBS

ORPHA:98918

Giant axonal neuropathy

GAN

ORPHA:643

Hereditary neuropathy with liability to pressure palsies

Current pressure-sensitive neuropathy · HNPP

ORPHA:640

Navajo neurohepatopathy

Navajo neuropathy

ORPHA:255229

Pudendal nerve entrapment syndrome

Alcock syndrome · Pudendal algia

ORPHA:60039