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"

12 matching diseasesClear search ×

Facial cleft

Craniofacial cleft

ORPHA:141229

Craniofacial conodysplasia

ORPHA:85168

Crouzon syndrome

Crouzon craniofacial dysostosis

ORPHA:207

Deafness-craniofacial syndrome

Hearing loss-craniofacial syndrome

ORPHA:3241

Diprosopus

Diprosopia · Craniofacial duplication

ORPHA:1681

Flat face-microstomia-ear anomaly syndrome

Blepharophimosis-telecanthus-microstomia syndrome · Simosa-Penchaszadeh-Bustos syndrome

ORPHA:1968

Genetic facial cleft

Genetic craniofacial cleft

ORPHA:414726

Lateral facial cleft

ORPHA:141269

Median facial cleft

Midline facial cleft · Tessier number 0-14 and 30 facial cleft

ORPHA:141234

Oblique facial cleft

Orbitofacial cleft

ORPHA:141253

Paramedian facial cleft

Tessier number 1-1 and 2-12 facial cleft

ORPHA:155867

Tessier number 7 facial cleft

Commissural facial cleft · Transverse facial cleft

ORPHA:141276