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 ×

PUM1-related cerebellar ataxia

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

ORPHA:642747

Adult-onset Steinert myotonic dystrophy

Adult-onset Steinert disease · Adult-onset myotonic dystrophy type 1

ORPHA:589830

Adult-onset Still disease

AOSD · Wissler-Fanconi syndrome

ORPHA:829

Carnitine palmitoyl transferase II deficiency, myopathic form

CPT2, myopathic form · CPTII, adult-onset form

ORPHA:228302

Ocular cystinosis

Adult-onset cystinosis · Non-nephropathic cystinosis

ORPHA:411641

Overlap myositis

Non-specific myositis · Adult-onset overlap myositis

ORPHA:206572

Primary lateral sclerosis

Adult-onset PLS · Adult-onset primary lateral sclerosis

ORPHA:35689

Young adult-onset distal hereditary motor neuropathy

Autosomal recessive distal spinal muscular atrophy type 5 · Young adult-onset dHMN

ORPHA:314485