Albinism-deafness syndrome
ORPHA:998Abruzzo-Erickson syndrome
ORPHA:921Ataxia-deafness-intellectual disability syndrome
ORPHA:1188Autosomal dominant deafness-onychodystrophy syndrome
ORPHA:79499Autosomal dominant optic atrophy plus syndrome
ORPHA:1215Bartter syndrome type 4
ORPHA:89938Bilateral microtia-deafness-cleft palate syndrome
ORPHA:140963Björnstad syndrome
ORPHA:123Branchiogenic deafness syndrome
ORPHA:50815Cataract-ataxia-deafness syndrome
ORPHA:1368Cataract-deafness-hypogonadism syndrome
ORPHA:1383Caudal appendage-deafness syndrome
ORPHA:1123Charcot-Marie-Tooth disease type 1E
ORPHA:90658Cleft lip/palate-deafness-sacral lipoma syndrome
ORPHA:2003Corneal dystrophy-perceptive deafness syndrome
ORPHA:1490Crandall syndrome
ORPHA:202Craniofacial-deafness-hand syndrome
ORPHA:1529Cutaneous mastocytosis-deafness-microtia syndrome
ORPHA:2135De Hauwere syndrome
ORPHA:1831Deafness with labyrinthine aplasia, microtia, and microdontia
ORPHA:90024Deafness-craniofacial syndrome
ORPHA:3241Deafness-ear malformation-facial palsy syndrome
ORPHA:3232Deafness-enamel hypoplasia-nail defects syndrome
ORPHA:3220Deafness-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:2143Dysmorphism-conductive hearing loss-heart defect syndrome
ORPHA:289553Epiphyseal dysplasia-hearing loss-dysmorphism syndrome
ORPHA:1825Fountain syndrome
ORPHA:3219Gemignani syndrome
ORPHA:2074Generalized resistance to thyroid hormone
ORPHA:3221Heart-hand syndrome
ORPHA:228184High myopia-sensorineural deafness syndrome
ORPHA:363396Hirschsprung disease-deafness-polydactyly syndrome
ORPHA:2155Hypospadias-hypertelorism-coloboma and deafness syndrome
ORPHA:157788Hypotrichosis-deafness syndrome
ORPHA:330029Jervell and Lange-Nielsen syndrome
ORPHA:90647Johnson neuroectodermal syndrome
ORPHA:2316KID syndrome
ORPHA:477Lowe-Kohn-Cohen syndrome
ORPHA:2408Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649Mitochondrial DNA-related cardiomyopathy and hearing loss
ORPHA:1349Mohr-Tranebjaerg syndrome
ORPHA:52368Multiple synostoses syndrome
ORPHA:3237