ORPHA:95464
Congenital mitral valve insufficiency and/or stenosis
- 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 | Congenital mitral valve insufficiency and/or stenosis | |
| fr | Insuffisance et/ou sténose de la valve mitrale | |
| de | Mitralklappeninsuffizienz oder -stenose, kongenitale | |
| es | Insuficiencia y/o estenosis valvular mitral congénita | |
| it | Insufficienza o stenosi congenita della valvola mitrale | |
| nl | Congenitale mitralisklepinsufficiëntie en/of -stenose | |
| pt | Insuficiência ou estenose congénita da válvula mitral | |
| pl | Wrodzona niewydolność i(lub) zwężenie zastawki mitralnej | |
| cs | Vrozená nedostatečnost a/nebo stenóza mitrální chlopně | |
| uk | Вроджена недостатність та/або стеноз мітрального клапана | |
| zh | 先天性二尖瓣关闭不全和/或狭窄 | |
| tr | Doğumsal mitral kapak yetmezliği ve/veya stenoz |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019817 | E | validated | |
| UMLS | C5681577 | 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 (1):
- ORPHA:2447Congenital mitral malformation
rare developmental anomalies during embryogenesis; rare cardiac malformations
Children (10):
- ORPHA:99061Accessory mitral valve tissue
- ORPHA:101932Anomaly of the mitral subvalvular apparatus
- ORPHA:99057Congenital mitral stenosis
- ORPHA:99059Congenital supravalvular mitral ring
- ORPHA:99060Congenital unguarded mitral orifice
- ORPHA:741Familial mitral valve prolapse
- ORPHA:99058Hypoplasia of the mitral valve annulus
- ORPHA:1205Mitral atresia
- ORPHA:99062Mitral valve agenesis
- ORPHA:99063Shone complex
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/95464
- This record as JSON: /data/d/95464.json