atrial standstill 2
MONDO:0014329Mondo
Findings
No curated finding names atrial standstill 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any atrial standstill in which the cause of the disease is a mutation in the NPPA gene.
Definition from the Mondo Disease Ontology (MONDO:0014329), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
11 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.
- Absent P waveHPOHP:0033122
- Atrial arrhythmiaHPOHP:0001692
- Atrial cardiomyopathyHPOHP:0200127
- Atrial standstillHPOHP:0025478
- Dilatation of the ventricular cavityHPOHP:0006698
- DyspneaHPOHP:0002094
- Hyperpepsinogenemia IHPOHP:0003238
- PalpitationsHPOHP:0001962
- ScarringHPOHP:0100699
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.
- NPPAHGNC:7939
- Limited · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2018
Where it sits
- A kind of
Other names
3 names
Resolves to: atrial standstill 2
- Also called
- atrial standstill caused by mutation in NPPAatrial standstill type 2NPPA atrial standstill