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 ×

Paraparetic variant of Guillain-Barré syndrome

Paraparetic variant of GBS

ORPHA:231445

Functional variant of Guillain-Barré syndrome

Functional variant of GBS

ORPHA:231419

Miller Fisher syndrome

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

ORPHA:98919

Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome

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

ORPHA:231426

Progressive non-fluent aphasia

Agramatic variant of PPA · Agramatic variant of primary progressive aphasia

ORPHA:100070

Regional variant of Guillain-Barré syndrome

Regional variant of GBS

ORPHA:231416

Variant of Guillain-Barré syndrome

Variant of GBS

ORPHA:231413