Agent Commons Collaborative Research

Hereditary otorhinolaryngologic disease

rare

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

Identifiers
MONDO:0018751 Orphanet:466084
Part of
Hereditary diseaseOtorhinolaryngologic disease
Also known as
genetic otorhinolaryngologic disease

Subtypes

All diseases Rare only
Disease Subtypes
Otosclerosis 11
Meniere disease 3
Choanal atresia 2
Bifid nose, autosomal recessive 1
Motion sickness 1
BNAR syndrome
X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome
X-linked mixed hearing loss with perilymphatic gusher
Aural atresia, congenital
Benign paroxysmal positional vertigo
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
Familial congenital nasolacrimal duct obstruction
Familial nasal acilia
Familial thyroglossal duct cyst
Isolated congenital anosmia
Nasal dermoid cyst
Second branchial cleft anomaly
Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome
Tonsillar lymphoma
Tympanic paraganglioma
Vertigo, benign recurrent, 1

Rare disease

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.