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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
102 clinical trials for this condition and its sub-types, 0 tagged with Hereditary otorhinolaryngologic disease itself.
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Browse by category โSub-types of Hereditary otorhinolaryngologic disease
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Benign paroxysmal positional vertigo 18 trials
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Meniere disease 16 trials
3 sub-types
- Active cochlear Meniere disease 0 trials
- Active cochleovestibular Meniere disease 0 trials
- Active vestibular Meniere disease 0 trials
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Motion sickness 14 trials ยท 16 incl. sub-types
1 sub-type
- Space motion sickness 4 trials
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Choanal atresia 4 trials
2 sub-types
- Choanal atresia, bilateral 0 trials
- Choanal atresia, unilateral 0 trials
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Otosclerosis 4 trials
11 sub-types
- Congenital corneal opacities, cornea guttata, and corectopia 0 trials
- Otosclerosis 1 0 trials
- Otosclerosis 10 0 trials
- Otosclerosis 11 0 trials
- Otosclerosis 12 0 trials
- Otosclerosis 2 0 trials
- Otosclerosis 3 0 trials
- Otosclerosis 4 0 trials
- Otosclerosis 5 0 trials
- Otosclerosis 7 0 trials
- Otosclerosis 8 0 trials
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Familial thyroglossal duct cyst 2 trials
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BNAR syndrome 1 trial
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Aural atresia, congenital 1 trial
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Second branchial cleft anomaly 1 trial
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Bifid nose, autosomal recessive 0 trials
1 sub-type
- Paramedian nasal cleft 0 trials
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Familial nasal acilia 0 trials
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Isolated congenital anosmia 0 trials
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Nasal dermoid cyst 0 trials
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Tonsillar lymphoma 0 trials
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Tympanic paraganglioma 0 trials
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Vertigo, benign recurrent, 1 0 trials
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