Branchiogenic deafness syndrome
ORPHA:50815Abruzzo-Erickson syndrome
ORPHA:921Albinism-deafness syndrome
ORPHA:998Bartter syndrome type 4
ORPHA:89938Bilateral microtia-deafness-cleft palate syndrome
ORPHA:140963Björnstad syndrome
ORPHA:123BOR syndrome
ORPHA:107Branchiootic syndrome
ORPHA:52429Branchioskeletogenital syndrome
ORPHA:1299Cataract-ataxia-deafness syndrome
ORPHA:1368Cataract-deafness-hypogonadism syndrome
ORPHA:1383Caudal appendage-deafness syndrome
ORPHA:1123Cleft lip/palate-deafness-sacral lipoma syndrome
ORPHA:2003Crandall syndrome
ORPHA:202Craniofacial-deafness-hand syndrome
ORPHA:1529Cutaneous mastocytosis-deafness-microtia syndrome
ORPHA:2135Deafness with labyrinthine aplasia, microtia, and microdontia
ORPHA:90024Deafness-craniofacial syndrome
ORPHA:3241Deafness-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:3239Duane retraction syndrome with congenital deafness
ORPHA:529574Generalized resistance to thyroid hormone
ORPHA:3221High myopia-sensorineural deafness syndrome
ORPHA:363396Hypotrichosis-deafness syndrome
ORPHA:330029Jervell and Lange-Nielsen syndrome
ORPHA:90647Mohr-Tranebjaerg syndrome
ORPHA:52368Multiple synostoses syndrome
ORPHA:3237Nephrotic syndrome-epidermolysis bullosa-sensorineural deafness syndrome
ORPHA:300333Neutropenia-monocytopenia-deafness syndrome
ORPHA:2690Palmoplantar keratoderma-deafness syndrome
ORPHA:2202Pendred syndrome
ORPHA:705Perrault syndrome
ORPHA:2855Postlingual non-syndromic genetic deafness
ORPHA:216452Prelingual non-syndromic genetic deafness
ORPHA:216445Rare syndromic genetic deafness
ORPHA:90642Renal caliceal diverticuli-deafness syndrome
ORPHA:2838Spastic paraparesis-deafness syndrome
ORPHA:2815Spastic paraplegia-nephritis-deafness syndrome
ORPHA:2820Split hand-split foot-deafness syndrome
ORPHA:71271Tietz syndrome
ORPHA:42665Usher syndrome
ORPHA:886X-linked spinocerebellar ataxia type 3
ORPHA:85297