autosomal dominant nocturnal frontal lobe epilepsy 2
Also known as: ENFL2, autosomal dominant nocturnal frontal lobe epilepsy type 2, epilepsy, nocturnal frontal lobe, 2, epilepsy, nocturnal frontal lobe, type 2, nocturnal frontal lobe epilepsy 2
Additional Disease Briefs
autosomal dominant nocturnal frontal lobe epilepsy 3
Also known as: CHRNB2 autosomal dominant nocturnal frontal lobe epilepsy, ENFL3, autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNB2, autosomal dominant nocturnal frontal lobe epilepsy type 3, epilepsy, nocturnal frontal lobe, 3, epilepsy, nocturnal frontal lobe, type 3, nocturnal frontal lobe epilepsy 3
autosomal dominant nocturnal frontal lobe epilepsy 4
Also known as: CHRNA2 autosomal dominant nocturnal frontal lobe epilepsy, ENFL4, autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNA2, autosomal dominant nocturnal frontal lobe epilepsy type 4, convulsions, benign familial infantile, 6, epilepsy, familial, with nocturnal wandering and Ictal fear, epilepsy, nocturnal frontal lobe, 4, epilepsy, nocturnal frontal lobe, type 4, nocturnal frontal lobe epilepsy 4, seizures, benign familial infantile, 6
autosomal dominant nocturnal frontal lobe epilepsy 5
Also known as: ENFL5, KCNT1 autosomal dominant nocturnal frontal lobe epilepsy, autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in KCNT1, autosomal dominant nocturnal frontal lobe epilepsy type 5, epilepsy nocturnal frontal lobe, 5, epilepsy, nocturnal frontal lobe, 5, epilepsy, nocturnal frontal lobe, type 5, nocturnal frontal lobe epilepsy 5
autosomal dominant nonsyndromic hearing loss
Also known as: autosomal dominant deafness, autosomal dominant isolated deafness, autosomal dominant isolated neurosensory deafness type DFNA, autosomal dominant isolated neurosensory hearing loss type DFNA, autosomal dominant isolated sensorineural deafness type DFNA, autosomal dominant isolated sensorineural hearing loss type DFNA, autosomal dominant non-syndromic neurosensory deafness type DFNA, autosomal dominant non-syndromic neurosensory hearing loss type DFNA, autosomal dominant non-syndromic sensorineural deafness type DFNA, autosomal dominant non-syndromic sensorineural hearing loss type DFNA, autosomal dominant nonsyndromic deafness, autosomal dominant nonsyndromic genetic deafness, autosomal dominant nonsyndromic hearing impairment, autosomal dominant nonsyndromic hearing loss, autosomal dominant nonsyndromic hearing loss and deafness, deafness, autosomal dominant, nonsyndromic deafness, autosomal dominant, nonsyndromic genetic deafness, autosomal dominant
autosomal dominant nonsyndromic hearing loss 1
Also known as: DFNA1, DIAPH1 autosomal dominant nonsyndromic deafness, Konigsmark syndrome, LFHL1, autosomal dominant deafness 1, autosomal dominant nonsyndromic deafness 1, autosomal dominant nonsyndromic deafness caused by mutation in DIAPH1, autosomal dominant nonsyndromic deafness type 1, deafness, autosomal dominant 1, deafness, autosomal dominant 1, with or without thrombocytopenia, deafness, autosomal dominant type 1, deafness, progressive Low tone, hereditary Low frequency hearing loss, hereditary low frequency hearing loss 1
autosomal dominant nonsyndromic hearing loss 10
Also known as: DFNA10, EYA4 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 10, autosomal dominant nonsyndromic deafness 10, autosomal dominant nonsyndromic deafness caused by mutation in EYA4, autosomal dominant nonsyndromic deafness type 10, autosomal dominant nonsyndromic hearing loss 10, deafness, autosomal dominant 10, deafness, autosomal dominant type 10
autosomal dominant nonsyndromic hearing loss 11
Also known as: DFNA11, MYO7A autosomal dominant nonsyndromic deafness, autosomal dominant deafness 11, autosomal dominant nonsyndromic deafness 11, autosomal dominant nonsyndromic deafness caused by mutation in MYO7A, autosomal dominant nonsyndromic deafness type 11, deafness, autosomal dominant 11, deafness, autosomal dominant type 11
autosomal dominant nonsyndromic hearing loss 12
Also known as: DFNA12, DFNA8, TECTA autosomal dominant nonsyndromic deafness, autosomal dominant deafness 12, autosomal dominant deafness 8, autosomal dominant nonsyndromic deafness 12, autosomal dominant nonsyndromic deafness caused by mutation in TECTA, autosomal dominant nonsyndromic deafness type 12, autosomal dominant nonsyndromic hearing loss 12, deafness, autosomal dominant 12, deafness, autosomal dominant 8, deafness, autosomal dominant 8/12, deafness, autosomal dominant type 12
autosomal dominant nonsyndromic hearing loss 13
Also known as: COL11A2 autosomal dominant nonsyndromic deafness, DFNA13, autosomal dominant deafness 13, autosomal dominant nonsyndromic deafness 13, autosomal dominant nonsyndromic deafness caused by mutation in COL11A2, autosomal dominant nonsyndromic deafness type 13, deafness, autosomal dominant 13, deafness, autosomal dominant type 13