Peripheral vertigo
diseaseOn this page
Summary
Peripheral vertigo (MONDO:0004900) is a disease with 6 GWAS associations across 6 studies and 3 clinical trials. Top therapeutic interventions include dimenhydrinate and sodium bicarbonate. A subtype of vestibular disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- GWAS associations: 6
- Clinical trials: 3
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | peripheral vertigo |
| Mondo ID | MONDO:0004900 |
| DOID | DOID:9847 |
| SNOMED CT | 50438001 |
| UMLS | C0155501 |
| MedGen | 102334 |
| Is cancer (heuristic) | no |
Data availability: 6 GWAS associations (6 studies).
Disease family
This is a subtype of vestibular disorder. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: disease › human disease › disease by body system or component › auditory system disorder › inner ear disorder › vestibular disorder › peripheral vertigo
Subtypes (4): endolymphatic hydrops, vertigo, benign recurrent, 2, benign paroxysmal positional vertigo, vertigo, benign recurrent, 1
Genetics & variants
GWAS landscape
6 GWAS associations across 6 studies. Top hits map to 2 distinct genes (as reported by GWAS).
Top associations by p-value
| rsID | p-value | Gene | Risk allele | Odds ratio |
|---|---|---|---|---|
| rs10862089 | 1e-30 | OTOGL | G | 0.24 |
| rs426564 | 2e-29 | ZNF91 | G | 0.14 |
| chr19:23486668 | 5e-24 | A | 0.15 | |
| rs2980097 | 1e-12 | TMEM128 - LYAR | C | 0.09 |
Top studies (by case count)
| Study | Lead author | Year | Cases | Controls | Title |
|---|---|---|---|---|---|
| GCST90475907 | Verma A | 2024 | 13,472 | 421,612 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90477814 | Verma A | 2024 | 2,768 | 115,422 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90480112 | Verma A | 2024 | 2,768 | 115,422 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90475906 | Verma A | 2024 | 1,863 | 55,550 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90436046 | Zhou W | 2018 | 380 | 402,827 | Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies. |
| GCST90043831 | Jiang L | 2021 | 284 | 456,064 | A generalized linear mixed model association tool for biobank-scale data. |
Variant details and genetic-evidence tiers
Tier distribution (top 50 variants)
| Tier | Variants |
|---|---|
| Tier 1: coding | 1 |
| Tier 2: splice/UTR | 0 |
| Tier 3: regulatory | 0 |
| Tier 4: intronic/intergenic | 3 |
MAF distribution
| Bucket | Variants |
|---|---|
| common (>=0.05) | 4 |
| low_freq (0.01-0.05) | 0 |
| rare (<0.01) | 0 |
| unknown | 0 |
Functional consequences
| Consequence | Count |
|---|---|
| intergenic_variant | 2 |
| missense_variant | 1 |
| unknown | 1 |
Top variants
| rsID | Chr | Pos | Alleles | MAF | Consequence | Gene | p-value | Tier |
|---|---|---|---|---|---|---|---|---|
| rs10862089 | 12 | 80305695 | G>T | 0.081 | missense_variant | OTOGL | 1e-30 | Tier 1: coding |
| rs426564 | 19 | 23314211 | G>A,C | 0.308 | intergenic_variant | ZNF91 | 2e-29 | Tier 4: intronic/intergenic |
| chr19:23486668 | 0.212 | 5e-24 | Tier 4: intronic/intergenic | |||||
| rs2980097 | 4 | 4251914 | C>A,G | 0.395 | intergenic_variant | TMEM128 - LYAR | 1e-12 | Tier 4: intronic/intergenic |
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 3.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE4 | 1 |
| PHASE3 | 1 |
| Not specified | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT01890538 | PHASE4 | COMPLETED | Comparison of Efficacy Between Piracetam and Dimenhydrinate in Patients With Peripheral Vertigo |
| NCT05586763 | PHASE3 | RECRUITING | Comparison of Efficacy of Metoclopramide , Promethazine and Prochloroperazine in the Treatment of Vertigo. |
| NCT05676216 | Not specified | UNKNOWN | Sodium Bicarbonate for Acute Peripheral Vertigo |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| DIMENHYDRINATE | 4 | 1 |
| SODIUM BICARBONATE | 4 | 1 |
Related Atlas pages
- Drugs: Dimenhydrinate, Sodium Bicarbonate