Craniofacial-deafness-hand syndrome
ORPHA:15293MC syndrome
ORPHA:293843Abruzzo-Erickson syndrome
ORPHA:921Albinism-deafness syndrome
ORPHA:998Arthrogryposis-like hand anomaly-sensorineural deafness syndrome
ORPHA:1144Bartter syndrome type 4
ORPHA:89938Bilateral microtia-deafness-cleft palate syndrome
ORPHA:140963Björnstad syndrome
ORPHA:123Branchiogenic deafness syndrome
ORPHA:50815Burn-McKeown syndrome
ORPHA:1200Cataract-ataxia-deafness syndrome
ORPHA:1368Cataract-deafness-hypogonadism syndrome
ORPHA:1383Caudal appendage-deafness syndrome
ORPHA:1123Charcot-Marie-Tooth disease type 1E
ORPHA:90658Cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome
ORPHA:508476Cleft lip/palate-deafness-sacral lipoma syndrome
ORPHA:2003Congenital hereditary facial paralysis-variable hearing loss syndrome
ORPHA:306530Corneal dystrophy-perceptive deafness syndrome
ORPHA:1490Crandall syndrome
ORPHA:202Craniofaciofrontodigital syndrome
ORPHA:363705Deafness with labyrinthine aplasia, microtia, and microdontia
ORPHA:90024Deafness-craniofacial syndrome
ORPHA:3241Deafness-ear malformation-facial palsy syndrome
ORPHA:3232Deafness-hypogonadism syndrome
ORPHA:90646Deafness-infertility syndrome
ORPHA:94064Deafness-lymphedema-leukemia syndrome
ORPHA:3226Deafness-oligodontia syndrome
ORPHA:3230Deafness-onychodystrophy syndrome
ORPHA:3231Deafness-vitiligo-achalasia syndrome
ORPHA:3239Donnai-Barrow syndrome
ORPHA:2143Flat face-microstomia-ear anomaly syndrome
ORPHA:1968Fountain syndrome
ORPHA:3219Heart-hand syndrome
ORPHA:228184Heart-hand syndrome type 2
ORPHA:1350Heart-hand syndrome type 3
ORPHA:1342High myopia-sensorineural deafness syndrome
ORPHA:363396Holt-Oram syndrome
ORPHA:392Hypospadias-hypertelorism-coloboma and deafness syndrome
ORPHA:157788Hypotrichosis-deafness syndrome
ORPHA:330029Jervell and Lange-Nielsen syndrome
ORPHA:90647Multiple synostoses syndrome
ORPHA:3237Neutropenia-monocytopenia-deafness syndrome
ORPHA:2690OBSOLETE: Cranioacrofacial syndrome
ORPHA:1339Orofacial clefting syndrome
ORPHA:139039Pendred syndrome
ORPHA:705Perrault syndrome
ORPHA:2855Rare syndromic genetic deafness
ORPHA:90642Renal caliceal diverticuli-deafness syndrome
ORPHA:2838