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"

18 matching diseasesClear search ×

Non-specific autoimmune cerebellar ataxia without characteristic antibodies

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

ORPHA:624268

Autosomal dominant cerebellar ataxia

ADCA · Autosomal dominant spinocerebellar ataxia

ORPHA:99

Autosomal dominant cerebellar ataxia type I

ADCA1 · ADCAI

ORPHA:94145

Autosomal dominant cerebellar ataxia type II

ADCA2 · ADCAII

ORPHA:208508

Autosomal dominant cerebellar ataxia type III

ADCA3 · ADCAIII

ORPHA:94148

Autosomal dominant cerebellar ataxia type IV

ADCA4 · ADCAIV

ORPHA:94149

Autosomal recessive ataxia due to ubiquinone deficiency

ARCA2 · Autosomal recessive ataxia due to coenzyme Q10 deficiency

ORPHA:139485

Autosomal recessive ataxia, Beauce type

SCAR8 · ARCA1

ORPHA:88644

Autosomal recessive cerebellar ataxia

ARCA

ORPHA:1172

Cerebellar ataxia, Cayman type

Cayman ataxia

ORPHA:94122

Immune-mediated cerebellar ataxia

IMCA · Autoimmune cerebellitis

ORPHA:623638

Non-specific autoimmune cerebellar ataxia with characteristic antibodies

Non-specific autoimmune CA with characteristic antibodies

ORPHA:624259

Paraneoplastic cerebellar degeneration

PCD · Subacute cerebellar degeneration

ORPHA:623626

Postinfectious cerebellitis

PIC · Para-infectious cerebellitis

ORPHA:624244

Primary autoimmune enteropathy

ORPHA:522037

PUM1-related cerebellar ataxia

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

ORPHA:642747

X-linked cerebellar ataxia

ORPHA:247765

X-linked progressive cerebellar ataxia

ORPHA:1175