hereditary otorhinolaryngologic disease
MONDO:0018751Mondo
Findings
No curated finding names hereditary otorhinolaryngologic disease yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An instance of otorhinolaryngologic disease that is caused by a modification of the individual's genome.
Definition from the Mondo Disease Ontology (MONDO:0018751), read 2026-09-29. CC BY 4.0.
Where it sits
- Narrower terms (21)
- aural atresia, congenital
- benign paroxysmal positional vertigo
- bifid nose, autosomal recessive
- BNAR syndrome
- cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
- choanal atresia
- familial congenital nasolacrimal duct obstruction
- familial nasal acilia
- familial thyroglossal duct cyst
- isolated congenital anosmia
- Meniere disease
- motion sickness
- nasal dermoid cyst
- otosclerosis
- second branchial cleft anomaly
- short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome
- tonsillar lymphoma
- tympanic paraganglioma
- vertigo, benign recurrent, 1
- X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome
- X-linked mixed hearing loss with perilymphatic gusher
Other names
1 name
Resolves to: hereditary otorhinolaryngologic disease
- Also called
- genetic otorhinolaryngologic disease