Hereditary otorhinolaryngologic disease
MONDO:0018751An instance of otorhinolaryngologic disease that is caused by a modification of the individual's genome.
Also known as: genetic otorhinolaryngologic disease
80 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)
Meniere disease
(13)
Benign paroxysmal positional vertigo
(12)
Motion sickness
(12)
Familial congenital nasolacrimal duct obstruction
(6)
Choanal atresia
(4)
Space motion sickness
(4)
Otosclerosis
(3)
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
(2)
Aural atresia, congenital
(1)
BNAR syndrome
(1)
Familial thyroglossal duct cyst
(1)
Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome
(1)
Active cochlear Meniere disease
(0)
Active cochleovestibular Meniere disease
(0)
Active vestibular Meniere disease
(0)
Bifid nose, autosomal recessive
(0)
Choanal atresia, bilateral
(0)
Choanal atresia, unilateral
(0)
Congenital corneal opacities, cornea guttata, and corectopia
(0)