Nonsyndromic genetic hearing loss
MONDO:0019497A disease characterized by hearing loss that is not part of a larger syndrome.
Also known as: nonsyndromic deafness, nonsyndromic hearing loss, nonsyndromic genetic hearing loss, familial deafness, isolated genetic deafness, non-syndromic genetic deafness, nonsyndromic genetic deafness
111 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
X-linked mixed hearing loss with perilymphatic gusher
(22)
Autosomal recessive nonsyndromic hearing loss 9
(7)
Postlingual non-syndromic genetic hearing loss
(6)
Prelingual non-syndromic genetic hearing loss
(5)
Deafness, aminoglycoside-induced
(4)
Autosomal recessive nonsyndromic hearing loss 1A
(2)
Autosomal recessive nonsyndromic hearing loss 39
(2)
Autosomal dominant nonsyndromic hearing loss
(1)
Autosomal dominant nonsyndromic hearing loss 9
(1)
Autosomal recessive nonsyndromic hearing loss 23
(1)
Autosomal recessive nonsyndromic hearing loss 5
(1)
Autosomal recessive nonsyndromic hearing loss 93
(1)
Hearing loss, autosomal recessive
(1)
Hearing loss, autosomal recessive 118, with cochlear aplasia
(1)
Autosomal dominant auditory neuropathy 1
(0)
Autosomal dominant nonsyndromic hearing loss 1
(0)
Autosomal dominant nonsyndromic hearing loss 10
(0)
Autosomal dominant nonsyndromic hearing loss 11
(0)
Autosomal dominant nonsyndromic hearing loss 12
(0)
Autosomal dominant nonsyndromic hearing loss 13
(0)