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"

17 matching diseasesClear search ×

Primary myelofibrosis

Agnogenic myeloid metaplasia · Idiopathic myelofibrosis

ORPHA:824

Acute panmyelosis with myelofibrosis

Acute myelodysplasia with myelofibrosis · Acute myelofibrosis

ORPHA:86843

Idiopathic avascular necrosis

Idiopathic AVN

ORPHA:399307

Idiopathic bronchiectasis

ORPHA:60033

Idiopathic eosinophilic myositis

Idiopathic eosinophilia-associated myopathy

ORPHA:247724

Idiopathic gastroparesis

ORPHA:558411

Idiopathic optic perineuritis

Idiopathic OPN

ORPHA:499107

Idiopathic peliosis hepatis

Idiopathic peliosis hepatitis

ORPHA:480524

Idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis · IPF

ORPHA:2032

Idiopathic scleritis

ORPHA:648675

Idiopathic small fibers neuropathy

Idiopathic-SFN

ORPHA:658549

Idiopathic spontaneous coronary artery dissection

Idiopathic SCAD

ORPHA:458718

Idiopathic steroid-resistant nephrotic syndrome

Idiopathic SRNS

ORPHA:567548

Idiopathic subglottic stenosis

iSGS

ORPHA:652681

Idiopathic syringomyelia

ORPHA:99858

IgG4-related retroperitoneal fibrosis

Ormond disease · Idiopathic retroperitoneal fibrosis

ORPHA:49041

Sporadic idiopathic steroid-resistant nephrotic syndrome

Sporadic idiopathic nephrosis

ORPHA:84271