ORPHA:101934
Genetic cardiac rhythm disease
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Genetic cardiac rhythm disease | |
| fr | Trouble génétique du rythme cardiaque | |
| de | Herzrythmusstörung, genetisch bedingte | |
| es | Enfermedad genética del ritmo cardíaco | |
| it | Malattia genetica del ritmo cardiaco | |
| nl | Genetische cardiale ritme-stoornis | |
| pt | Doença do ritmo cardíaco, genética | |
| pl | Genetyczne choroby zaburzenia rytmu serca | |
| cs | Geneticky podmíněná onemocnění srdečního rytmu | |
| uk | Генетично обумовлене захворювання серцевого ритму | |
| zh | 遗传性心律失常 | |
| tr | Genetik kalp ritmi hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15110 | E | validated | |
| UMLS | C5681782 | E | validated | |
| GARD | 19785 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:218436Rare cardiac rhythm disease
rare cardiac diseases - ORPHA:98054Rare genetic cardiac disease
rare genetic diseases
Children (31):
- ORPHA:37553Andersen-Tawil syndrome
- ORPHA:1479Atrial septal defect-atrioventricular conduction defects syndrome
- ORPHA:476084BVES-related limb-girdle muscular dystrophy
- ORPHA:2946Brachydactyly-long thumb syndrome
- ORPHA:130Brugada syndrome
- ORPHA:726788Calcium release deficiency syndrome
- ORPHA:3286Catecholaminergic polymorphic ventricular tachycardia
- ORPHA:435988Chronic atrial and intestinal dysrhythmia syndrome
- ORPHA:60041Congenital heart block
- ORPHA:768Congenital long QT syndrome
- ORPHA:51083Congenital short QT syndrome
- ORPHA:728619Early repolarization syndrome
- ORPHA:542306GNB5-related intellectual disability-cardiac arrhythmia syndrome
- ORPHA:1350Heart-hand syndrome type 2
- ORPHA:1342Heart-hand syndrome type 3
- ORPHA:168796Heart-hand syndrome, Slovenian type
- ORPHA:334Hereditary atrial fibrillation
- ORPHA:436242Hereditary atrial tachyarrhythmia-infra-Hisian cardiac conduction disease
- ORPHA:871Hereditary progressive cardiac conduction defect
- ORPHA:166282Hereditary sick sinus syndrome
- ORPHA:3283His bundle tachycardia
- ORPHA:137675Histiocytoid cardiomyopathy
- ORPHA:392Holt-Oram syndrome
- ORPHA:228140Idiopathic ventricular fibrillation
- ORPHA:1344Isolated atrial standstill
- ORPHA:723139Multifocal ectopic Purkinje-related premature contraction
- ORPHA:228012Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome
- ORPHA:480864Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome
- ORPHA:324321Sinoatrial node dysfunction and deafness
- ORPHA:51084Torsade-de-pointes syndrome with short coupling interval
- ORPHA:324410X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome
Codes that Orphanet moved or referred to this one:
- ORPHA:844OBSOLETE: Lown-Ganong-Levine syndrome referred to · inactive
- ORPHA:99648OBSOLETE: Non-progressive congenital heart block referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/101934
- This record as JSON: /data/d/101934.json