OBSOLETE: Neurosensory deafness-pituitary dwarfism syndrome
ORPHA:3228Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome
ORPHA:538574Polyneuropathy-hearing loss-ataxia-retinitis pigmentosa-cataract syndrome
ORPHA:171848Progressive autosomal recessive ataxia-deafness syndrome
ORPHA:448251Progressive 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:90641Rare X-linked non-syndromic sensorineural deafness type DFN
ORPHA:90625Reticular dysgenesis
ORPHA:33355Sensorineural deafness with dilated cardiomyopathy
ORPHA:217622Sensorineural hearing loss-early graying-essential tremor syndrome
ORPHA:66633Sensorineural hearing loss-spastic quadriplegia-intellectual disability syndrome
ORPHA:659975Spondyloepiphyseal dysplasia, MacDermot type
ORPHA:163668Sudden sensorineural hearing loss
ORPHA:90059Syndromic hereditary optic neuropathy
ORPHA:441434Syndromic sensorineural deafness due to combined oxidative phosphorylation defect
ORPHA:457223X-linked Charcot-Marie-Tooth disease
ORPHA:64747X-linked hereditary sensory and autonomic neuropathy with deafness
ORPHA:139583