Vestibular dysfunction

Symptom Information:

Symptom ID: HPO:0001751
Synonyms:
Impaired vestibular function [HPO:0001751]
Interictal vestibular dysfunction [HPO:0001751]
Vestibular function defect [HPO:0001751]
Impaired vestibular function [OMIM:Impaired vestibular function]
Interictal vestibular dysfunction [OMIM:Interictal vestibular dysfunction]
Vestibular dysfunction [OMIM:Vestibular dysfunction]
Vestibular dysfunction (in some patients) [OMIM:Vestibular dysfunction (in some patients)]
Vestibular function defect (decreased in some, normal in other patients) [OMIM:Vestibular function defect (decreased in some, normal in other patients)]
Quality:
Cross references:
OMIM: "Impaired vestibular function" [OMIM:Impaired vestibular function]
OMIM: "Interictal vestibular dysfunction" [OMIM:Interictal vestibular dysfunction]
OMIM: "Vestibular dysfunction" [OMIM:Vestibular dysfunction]
OMIM: "Vestibular dysfunction (in some patients)" [OMIM:Vestibular dysfunction (in some patients)]
OMIM: "Vestibular function defect (decreased in some, normal in other patients)" [OMIM:Vestibular function defect (decreased in some, normal in other patients)]
Is a (Direct Parents):
HPO         Functional abnormality of the inner ear
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the ear(HPO:0000598)
          Abnormality of the inner ear(HPO:0000359)
             Functional abnormality of the inner ear(HPO:0011389)
                Vestibular dysfunction(HPO:0001751)
MedDRA:
Database Frequency: 19 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive nonsyndromic sensorineural deafness type DFNB (Orphanet:90636)
DEAFNESS, AUTOSOMAL RECESSIVE 1A (OMIM:220290)
DEAFNESS, AUTOSOMAL RECESSIVE 1B (OMIM:612645)
DEAFNESS, AUTOSOMAL RECESSIVE 2 (OMIM:600060)
DEAFNESS, AUTOSOMAL RECESSIVE 37 (OMIM:607821)
DEAFNESS, AUTOSOMAL RECESSIVE 48 (OMIM:609439)
DEAFNESS, AUTOSOMAL RECESSIVE 84A (OMIM:613391)
Familial paroxysmal ataxia (Orphanet:97)
Jervell and Lange-Nielsen syndrome (Orphanet:90647)
MELAS (Orphanet:550)
Maternally-inherited diabetes and deafness (Orphanet:225)
Pendred syndrome (Orphanet:705)
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis (Orphanet:70595)
Spinocerebellar ataxia with epilepsy (Orphanet:254881)
USHER SYNDROME, TYPE ID (OMIM:601067)
USHER SYNDROME, TYPE IG (OMIM:606943)
USHER SYNDROME, TYPE IJ (OMIM:614869)
USHER SYNDROME, TYPE IK (OMIM:614990)
Usher syndrome type 3 (Orphanet:231183)