Rare X-linked non-syndromic sensorineural deafness type DFN
ORPHA:90625Deafness with labyrinthine aplasia, microtia, and microdontia
ORPHA:90024Deafness-intellectual disability syndrome, Martin-Probst type
ORPHA:85321Hereditary sensory neuropathy-deafness-dementia syndrome
ORPHA:456318Mitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposure
ORPHA:168609OBSOLETE: Neurosensory deafness-pituitary dwarfism syndrome
ORPHA:3228Postlingual non-syndromic genetic deafness
ORPHA:216452Prelingual non-syndromic genetic deafness
ORPHA:216445Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome
ORPHA:228012Rare autosomal dominant non-syndromic sensorineural deafness type DFNA
ORPHA:90635Rare autosomal recessive non-syndromic sensorineural deafness type DFNB
ORPHA:90636Rare mitochondrial non-syndromic sensorineural deafness
ORPHA:90641Syndromic sensorineural deafness due to combined oxidative phosphorylation defect
ORPHA:457223X-linked hereditary sensory and autonomic neuropathy with deafness
ORPHA:139583X-linked mixed deafness with perilymphatic gusher
ORPHA:383X-linked neurodegenerative syndrome, Hamel type
ORPHA:85336X-linked spinocerebellar ataxia type 3
ORPHA:85297