Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandVertigo (D014717)
..Starting node
..expandBenign Paroxysmal Positional Vertigo (D065635)

       Child Nodes:



 Sister Nodes: 
..expandBenign Paroxysmal Positional Vertigo (D065635)
..expandEpisodic Ataxia, Type 3 (C564697)
..expandVertigo, Benign Recurrent (C562859)
..expandVertigo, Benign Recurrent, 1 (C567620)
..expandVertigo, Benign Recurrent, 2 (C567749)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:1218
Name:Benign Paroxysmal Positional Vertigo
Definition:Idiopathic recurrent VERTIGO associated with POSITIONAL NYSTAGMUS. It is associated with a vestibular loss without other neurological or auditory signs. Unlike in LABYRINTHITIS and VESTIBULAR NEURONITIS inflammation in the ear is not observed.
Alternative IDs:OMIM:193007
ParentIDs:MESH:D014717
TreeNumbers:C09.218.568.900.883.500 |C10.597.951.500 |C23.888.592.958.500
Synonyms:Benign Recurrent Vertigo |Benign Recurrent Vertigos |BPPV |BRV |BRV1, INCLUDED |Familial Benign Recurrent Vertigo |Familial Vestibulopathies |Familial Vestibulopathy |Recurrent Vertigo, Benign |Recurrent Vertigos, Benign |Vertigo, Benign Paroxysmal Positional |VERT
Slim Mappings:Ear-nose-throat disease|Nervous system disease|Signs and symptoms
Reference: MedGen: D065635
MeSH: D065635
OMIM: 193007;

Genes:
Phenotypes
1 HP:0000006Autosomal dominant inheritance
2 HP:0002141Gait imbalance
3 HP:0003677Slowly progressive
4 HP:0002321Vertigo
Disease Causing ClinVar Variants