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 ×

Paraneoplastic cerebellar degeneration

PCD · Subacute cerebellar degeneration

ORPHA:623626

Cerebellar hypoplasia-tapetoretinal degeneration syndrome

ORPHA:2246

Cerebellar malformation

ORPHA:182061

Genetic cerebellar malformation

ORPHA:269560

Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome

Dykes-Marks-Harper syndrome

ORPHA:2274

Infantile cerebellar-retinal degeneration

ORPHA:313850

Postinfectious cerebellitis

PIC · Para-infectious cerebellitis

ORPHA:624244

Spinocerebellar degeneration-corneal dystrophy syndrome

Der Kaloustian-Jarudi-Khoury syndrome

ORPHA:3177