SE-ATLAS

Rare deafness Usher syndrome Rare X-linked non-syndromic sensorineural deafness type DFN Syndromic sensorineural deafness due to combined oxidative phosphorylation defect Rare autosomal dominant non-syndromic sensorineural deafness type DFNA Rare autosomal recessive non-syndromic sensorineural deafness type DFNB Rare mitochondrial non-syndromic sensorineural deafness Syndromic genetic deafness Jervell and Lange-Nielsen syndrome MELAS Muckle-Wells syndrome Full NF2-related schwannomatosis Branchiogenic deafness syndrome Mohr-Tranebjaerg syndrome Conductive deafness-malformed external ear syndrome Deafness-ear malformation-facial palsy syndrome Bilateral microtia-deafness-cleft palate syndrome Mitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposure Pendred syndrome Sinoatrial node dysfunction and deafness Neuropathy with hearing impairment Fetal cytomegalovirus syndrome Perrault syndrome Susac syndrome Treacher-Collins syndrome DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome Goldenhar syndrome Waardenburg syndrome type 1 Wolfram syndrome Cogan syndrome Albinism-deafness syndrome Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome Spastic paraparesis-deafness syndrome Wolf-Hirschhorn syndrome Stickler syndrome Non-syndromic genetic deafness Townes-Brocks syndrome Congenital hereditary facial paralysis-variable hearing loss syndrome Waardenburg syndrome Prelingual non-syndromic genetic deafness Postlingual non-syndromic genetic deafness Wolfram-like syndrome Noonan syndrome with multiple lentigines