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 ×

Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome

PCB variant of GBS · PCB variant of Guillain-Barré syndrome

ORPHA:231426

Facial diplegia with paresthesias

Facial diplegia with paresthesias variant of Guillain-Barré syndrome · Facial diplegia with paresthesias variant of GBS

ORPHA:480701

Functional variant of Guillain-Barré syndrome

Functional variant of GBS

ORPHA:231419

Guillain-Barré syndrome

GBS · Guillain-Barré-Strohl syndrome

ORPHA:2103

Miller Fisher syndrome

Cranial variant of GBS · Cranial variant of Guillain-Barré syndrome

ORPHA:98919

Paraparetic variant of Guillain-Barré syndrome

Paraparetic variant of GBS

ORPHA:231445

Regional variant of Guillain-Barré syndrome

Regional variant of GBS

ORPHA:231416

Variant of Guillain-Barré syndrome

Variant of GBS

ORPHA:231413