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"

14 matching diseasesClear search ×

Paraneoplastic cerebellar degeneration

PCD · Subacute cerebellar degeneration

ORPHA:623626

Autosomal dominant cerebellar ataxia

ADCA · Autosomal dominant spinocerebellar ataxia

ORPHA:99

Cerebellar ataxia, Cayman type

Cayman ataxia

ORPHA:94122

Episodic ataxia type 4

PATX · Periodic vestibulocerebellar ataxia

ORPHA:79136

Immune-mediated cerebellar ataxia

IMCA · Autoimmune cerebellitis

ORPHA:623638

Non-specific autoimmune cerebellar ataxia without characteristic antibodies

Non-specific autoimmune CA without characteristic antibodies · Primary Autoimmune Cerebellar Ataxia

ORPHA:624268

Opsoclonus-myoclonus syndrome

Ataxo-opso-myoclonus syndrome · Dancing eye syndrome

ORPHA:1183

Paraneoplastic pemphigus

ORPHA:63455

Paraneoplastic uveitis

ORPHA:279928

Postinfectious cerebellitis

PIC · Para-infectious cerebellitis

ORPHA:624244

PUM1-related cerebellar ataxia

Adult-onset SCA47 · Adult-onset spinocerebellar ataxia type 47

ORPHA:642747

Sporadic adult-onset ataxia of unknown etiology

Idiopathic late-onset cerebellar ataxia · SAOA

ORPHA:247234

X-linked cerebellar ataxia

ORPHA:247765

X-linked progressive cerebellar ataxia

ORPHA:1175