Interventricular septum aneurysm
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
Interventricular septum aneurysm is a rare, non-syndromic, congenital heart malformation characterized by the presence of a congenital aneurysm of the membranous portion of the interventricular septum. Patients may be asymptomatic or may present with ventricular or supraventricular tachycardia, fatigue, exertional dyspnea, palpitations, and cardiac murmur. Ventricular septal defects and conduction defects, such as first-degree atrio-ventricular block or incomplete right bundle branch block, may also be also associated.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Interventricular septum aneurysm | |
| fr | Anévrisme du septum interventriculaire | |
| de | Septumaneurysma, interventrikuläres | |
| es | Aneurisma del septo interventricular | |
| it | Aneurisma del setto interventricolare | |
| nl | Interventriculair septumaneurysma | |
| pt | Aneurisma do septo intraventricular | |
| pl | Tętniak przegrody międzykomorowej | |
| cs | Aneuryzma mezikomorového septa | |
| uk | Аневризма міжшлуночкової перегородки | |
| zh | 室间隔动脉瘤 | |
| tr | İnterventriküler septum anevrizması |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 105805 | E | validated | |
| ICD-10 | Q21.0 | NTBT | attributed | validated |
| ICD-11 | LA88.Y | NTBT | attributed | validated |
| MONDO | 0007112 | E | validated | |
| MeSH | C563239 | E | validated | |
| UMLS | C1387721 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:474347Rare congenital anomaly of ventricular septum
rare developmental anomalies during embryogenesis; rare cardiac malformations
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/99092
- This record as JSON: /data/d/99092.json