Hearing Loss Disease Portal


 
Switch to table view
Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandVestibulocochlear Nerve Diseases (D000160)
..Starting node
..expandVestibulocochlear Dysfunction, Progressive (C536346)

       Child Nodes:



 Sister Nodes: 
..expandCogan Syndrome (D055952) Child2
..expandDeafness, X-Linked 5 (C564472)
..expandNeuroma, Acoustic (D009464) Child1
..expandVestibular Neuronitis (D020338)
..expandVestibulocochlear Dysfunction, Progressive (C536346)
..expandVestibulocochlear Nerve Injuries (D061285)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:11601
Name:Vestibulocochlear Dysfunction, Progressive
Definition:
Alternative IDs:
ParentIDs:MESH:D000160
TreeNumbers:C09.218.807.800/C536346 |C10.292.910/C536346
Synonyms:Familial progressive vestibulo-cochlear dysfunction |Familial progressive vestibulocochlear dysfunction |Vestibulocochlear dysfunction progressive familial
Slim Mappings:Ear-nose-throat disease|Nervous system disease
Reference: MedGen: C536346
MeSH: C536346
OMIM: 193005;

Genes:
Phenotypes
1 HP:0000006Autosomal dominant inheritance
2 HP:0000707Abnormality of the nervous system
3 HP:0001730Progressive hearing impairment
4 HP:0000360Tinnitus
5 HP:0008568Vestibular areflexia
Disease Causing ClinVar Variants