Rare autosomal dominant non-syndromic sensorineural deafness type DFNA
ORPHA:90635Autosomal 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 Robinow syndrome
ORPHA:3107MME-related autosomal dominant Charcot Marie Tooth disease type 2
ORPHA:497757Rare 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:90625