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"

16 matching diseasesClear search ×

Guillain-Barré syndrome

GBS · Guillain-Barré-Strohl syndrome

ORPHA:2103

Acute motor and sensory axonal neuropathy

AMSAN · Acute motor-sensory axonal GBS

ORPHA:98917

Acute motor axonal neuropathy

AMAN · Acute pure motor GBS

ORPHA:98918

Acute pandysautonomia

Acute panautonomic GBS · Acute panautonomic Guillain-Barré syndrome

ORPHA:231457

Acute pure sensory neuropathy

Acute pure sensory GBS · Acute pure sensory Guillain-Barré syndrome

ORPHA:231450

Acute sensory ataxic neuropathy

ASAN · Acute sensory ataxic GBS

ORPHA:231466

Barth syndrome

3-methylglutaconic aciduria type 2 · BTHS

ORPHA:111

Frey syndrome

Baillarger syndrome · Auriculotemporal syndrome

ORPHA:662240

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

Paraparetic variant of Guillain-Barré syndrome

Paraparetic variant of GBS

ORPHA:231445

Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome

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

ORPHA:231426

Regional variant of Guillain-Barré syndrome

Regional variant of GBS

ORPHA:231416

Stromme syndrome

Jejunal atresia-microcephaly-ocular anomalies syndrome · Apple-peel intestinal atresia-ocular anomalies-microcephaly syndrome

ORPHA:506307

Thoracolaryngopelvic dysplasia

Barnes syndrome

ORPHA:3317

Variant of Guillain-Barré syndrome

Variant of GBS

ORPHA:231413