VESTIBULOCOCHLEAR DYSFUNCTION, PROGRESSIVE

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 6
OrphanetNr:
OMIM Id: 193005
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0001730) Progressive hearing impairment 29 / 7739
2
(HPO:0000360) Tinnitus 29 / 7739
3
(HPO:0008568) Vestibular areflexia 5 / 7739
4
(HPO:0000707) Abnormality of the nervous system 61 / 7739
5
(OMIM) Head movement-dependent oscillopsia and dark instability 1 / 7739
6
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: