autosomal dominant vibratory urticaria
Findings
No curated finding names autosomal dominant vibratory urticaria yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An autosomal dominant disease characterized by localized hives and systemic manifestations in response to dermal vibration, with coincident degranulation of mast cells and increased histamine levels in serum.
Definition from the Mondo Disease Ontology (MONDO:0007447), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
4 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Facial erythemaHPOHP:0001041
- 9 of 9 reported patients
- FlushingHPOHP:0031284
- 9 of 9 reported patients
- UrticariaHPOHP:0001025
- 9 of 9 reported patients
- Dermatographic urticariaHPOHP:0011971
- 0 of 9 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- ADGRE2HGNC:3337
- Supportive · Orphanet · Autosomal dominant · 2021
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2017
- Limited · G2P · Autosomal dominant · 2025
Where it sits
Other names
4 names
Resolves to: autosomal dominant vibratory urticaria
- Also called
- DDUdermodistortive urticariaVBUvibratory urticaria, autosomal dominant