ORPHA:95465
Cleft mitral valve
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare, congenital, non-syndromic heart malformation characterized by a slit-like hole or defect in one of the mitral valve leaflets, which is usually thickened and distorted. It usually affects the anterior leaflet, but the cleft of posterior leaflet has also been described. Cleft mitral valve can be isolated or associated with other congenital heart anomalies.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Cleft mitral valve | |
| fr | Fente mitrale | |
| de | Mitralklappenspalt | |
| es | Válvula mitral hendida | |
| it | Schisi della valvola mitrale | |
| nl | Gespleten mitralisklep | |
| pt | Fenda da Válvula mitral | |
| pl | Rozszczep zastawki mitralnej | |
| cs | Rozštěp mitrální chlopně | |
| uk | Розщеплення стулки мітрального клапана | |
| zh | 二尖瓣裂 | |
| tr | Yarık mitral kapak |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q23.3 | NTBT | attributed | validated |
| ICD-11 | LA87.1Y | NTBT | attributed | validated |
| MONDO | 0019818 | E | validated | |
| UMLS | C0344772 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:2447Congenital mitral malformation
rare developmental anomalies during embryogenesis; rare cardiac malformations
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/95465
- This record as JSON: /data/d/95465.json