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"

9 matching diseasesClear search ×

Fibromuscular dysplasia of the cervical and intracranial arteries

Cerebrovascular fibromuscular dysplasia · Cerebrovascular FMD

ORPHA:698036

Carotid web

AFMD · CaW

ORPHA:698260

Cerebral cortical dysplasia

Brain cortical dysplasia

ORPHA:268950

Cerebrofaciothoracic dysplasia

Pascual-Castroviejo syndrome type 1

ORPHA:1394

Fibromuscular dysplasia

FMD

ORPHA:698012

Fibromuscular dysplasia of the arteries of the extremities

Fibromuscular dysplasia of the arteries of the limbs · Limb fibromuscular dysplasia

ORPHA:698069

Fibromuscular dysplasia of the coronary arteries

Epicardial coronary artery fibromuscular dysplasia

ORPHA:698059

Fibromuscular dysplasia of the renal arteries

Renal artery fibromuscular dysplasia · Renal FMD

ORPHA:698043

Fibromuscular dysplasia of the visceral arteries

Visceral fibromuscular dysplasia

ORPHA:698063