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Up to: Hereditary disease · Otorhinolaryngologic disease

Hereditary otorhinolaryngologic disease

An instance of otorhinolaryngologic disease that is caused by a modification of the individual's genome.

0 trials tagged with this condition →

X-linked mixed hearing loss with perilymphatic gusher 32 trials
Benign paroxysmal positional vertigo 18 trials
Meniere disease 16 trials Sub-types →
Motion sickness 14 trials · 16 incl. sub-types Sub-types →
Familial congenital nasolacrimal duct obstruction 7 trials
Choanal atresia 4 trials Sub-types →
Otosclerosis 4 trials Sub-types →
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome 2 trials
Familial thyroglossal duct cyst 2 trials
BNAR syndrome 1 trial
Aural atresia, congenital 1 trial
Second branchial cleft anomaly 1 trial
Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome 1 trial
X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome 0 trials
Bifid nose, autosomal recessive 0 trials Sub-types →
Familial nasal acilia 0 trials
Isolated congenital anosmia 0 trials
Nasal dermoid cyst 0 trials
Tonsillar lymphoma 0 trials
Tympanic paraganglioma 0 trials
Vertigo, benign recurrent, 1 0 trials