Rare autosomal dominant non-syndromic sensorineural deafness type DFNA
ORPHA:90635Arthrogryposis-like hand anomaly-sensorineural deafness syndrome
ORPHA:1144Autosomal dominant Alport syndrome
ORPHA:88918Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome
ORPHA:314404Autosomal dominant deafness-onychodystrophy syndrome
ORPHA:79499Autosomal dominant dopa-responsive dystonia
ORPHA:98808Autosomal dominant hereditary sensory and autonomic neuropathy
ORPHA:140474Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome
ORPHA:440354Autosomal dominant non-syndromic intellectual disability
ORPHA:178469Autosomal dominant optic atrophy and congenital deafness
ORPHA:3212Bartter syndrome type 4
ORPHA:89938Crandall syndrome
ORPHA:202DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome
ORPHA:494444EAST syndrome
ORPHA:199343Ectodermal dysplasia-sensorineural deafness syndrome
ORPHA:1883Hereditary sensory neuropathy-deafness-dementia syndrome
ORPHA:456318High myopia-sensorineural deafness syndrome
ORPHA:363396Mitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposure
ORPHA:168609Progressive autosomal recessive ataxia-deafness syndrome
ORPHA:448251Rare autosomal recessive non-syndromic sensorineural deafness type DFNB
ORPHA:90636Rare mitochondrial non-syndromic sensorineural deafness
ORPHA:90641Rare X-linked non-syndromic sensorineural deafness type DFN
ORPHA:90625Reticular dysgenesis
ORPHA:33355Sensorineural hearing loss-early graying-essential tremor syndrome
ORPHA:66633Sudden sensorineural hearing loss
ORPHA:90059Syndromic sensorineural deafness due to combined oxidative phosphorylation defect
ORPHA:457223