Mesocardia
Synonyms: Midline heart
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare, congenital non-syndromic heart malformation characterized by an atypical location of the heart in a central position within the thorax, with the apex situated in the midline. The atrial arrangement is usually normal, whereas the ventricles may be inverted. Various congenital heart anomalies have also been associated, such as congenitally corrected transposition of the great arteries.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Mesocardia | Midline heart |
| fr | Mésocardie | |
| de | Mesokardie | |
| es | Mesocardia | Corazón en la línea media |
| it | Mesocardia | Cuore mediano |
| nl | Mesocardie | Hart in middellijn |
| pt | Mesocardia | |
| pl | Mezokardia | Serce położone pośrodkowo |
| cs | Mezokardie | Srdce ve střední čáře |
| uk | Мезокардія | Серединне серце |
| zh | 中位心 | 中位心 |
| tr | Mezokardi | Orta çizgi kalp |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q24.8 | NTBT | attributed | validated |
| ICD-11 | LA80.2 | E | specific | validated |
| MONDO | 0019807 | E | validated | |
| UMLS | C0265865 | 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:98716Heart position anomaly
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/95443
- This record as JSON: /data/d/95443.json