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"

3 matching diseasesClear search ×

Oculoauriculovertebral spectrum with radial defects

Hemifacial microsomia-radial defects syndrome · Moeschler-Clarren syndrome

ORPHA:2549

Oculo-auriculo-vertebral spectrum

OAV spectrum · Oculoauriculovertebral spectrum

ORPHA:141132

Goldenhar syndrome

Facioauriculovertebral sequence

ORPHA:374