Absence of innominate vein
Synonyms: Absence of brachiocephalic vein
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare congenital anomaly of the great veins characterized by absence of the left brachiocephalic vein (or innominate vein), resulting in an anomalous venous vasculature. Patients are usually asymptomatic and the anomaly is typically discovered intraoperatively. An association with persistence of left superior vena cava, permanent levoatrial cardinal vein or anomaly of the inferior vena cava has been reported in some cases.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Absence of innominate vein | Absence of brachiocephalic vein |
| fr | Absence de veine innominée | Absence de veine brachiocéphalique |
| de | Fehlen der Kopf-Armvene | Fehlen der Vena innominata · Vena brachiocephalica, fehlende |
| es | Ausencia de vena innominada | |
| it | Aplasia della vena anonima | |
| nl | Afwezigheid van vena brachiocephalica | Afwezigheid van arm-hoofdader · Afwezigheid van brachiocefalische ader |
| pt | Ausência de veia inominada | |
| pl | Brak żyły bezimmiennej | Brak żyły ramienno-głowowej |
| cs | Chybění vena innominata | Chybění vena brachiocefalica |
| uk | Відсутність безіменної вени | Відсутність брахіоцефальної вени |
| zh | 无名静脉缺失 | 头臂静脉缺如 |
| tr | Innominate ven yokluğu | Brakiyosefalik ven yokluğu |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q26.8 | NTBT | attributed | validated |
| ICD-11 | LA86.Y | NTBT | attributed | validated |
| MONDO | 0020443 | E | validated | |
| UMLS | C4707656 | 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:95498Congenital anomaly of superior vena cava
rare developmental anomalies during embryogenesis; rare cardiac malformations; rare circulatory system diseases
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/99112
- This record as JSON: /data/d/99112.json