Fixed subaortic stenosis
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- No data available
- Age of onset
- Childhood
- Status
- active
Fixed subaortic stenosis (FSS) is a rare heart malformation characterized by the obstruction by membranous or fibromuscular tissue of the left ventricular outflow tract (LVOT) below the aortic valve, that occurs as an isolated lesion or in association with additional cardiac malformations (e.g. ventricular septal defect, patent ductus arteriosus, coarctation of the aorta), that presents in childhood with signs of LVOT obstruction (e.g. dyspnea, chest pain, syncope, palpitations) and that can potentially lead to life-threatening complications (e.g. aortic regurgitation, infective endocarditis). It comprises three anatomical subforms: discrete fixed membranous subaortic stenosis (membranous tissue encircling the LVOT), discrete fibromuscular subaortic stenosis (fibromuscular tissue encircling the LVOT) and tunnel subaortic stenosis (fibromuscular diffuse tunnel-like narrowing of the LVOT), the two latter forms being generally more severe than the membranous form.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Fixed subaortic stenosis | |
| fr | Rétrécissement aortique sous-valvulaire | |
| de | Subaortenstenose, fixierte | |
| es | Estenosis subaórtica fija | |
| it | Stenosi subaortica fissa | |
| nl | Gefixeerde subaortastenose | |
| pt | Estenose subaórtica fixa | |
| pl | Zwężenie podaortalne | |
| cs | Fixovaná subaortální stenóza | |
| uk | Фіксований субаортальний стеноз | |
| zh | 主动脉瓣下固定性狭窄 | |
| tr | Sabit subaortik stenozu |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 271950 | BTNT | validated | |
| ICD-10 | Q24.4 | E | specific | validated |
| ICD-11 | LA8A.5 | NTBT | index | validated |
| MONDO | 0017727 | E | validated | |
| UMLS | C0265853 | 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:98718Aortic malformation
rare developmental anomalies during embryogenesis; rare cardiac malformations; rare circulatory system diseases
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
28 annotations · validated 2021-08-19| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Frequent (79-30%) | ||
| HP:0001627 | Abnormal heart morphology | |
| HP:0001659 | Aortic regurgitation | |
| HP:0001635 | Congestive heart failure | |
| HP:0031668 | Diastolic heart murmur | |
| HP:0002094 | Dyspnea | |
| HP:0002875 | Exertional dyspnea | |
| HP:0001712 | Left ventricular hypertrophy | |
| HP:0032092 | Left ventricular outflow tract obstruction | |
| HP:0001643 | Patent ductus arteriosus | |
| HP:0031664 | Systolic heart murmur | |
| HP:0001629 | Ventricular septal defect | |
| Occasional (29-5%) | ||
| HP:0001671 | Abnormal cardiac septum morphology | |
| HP:0001681 | Angina pectoris | |
| HP:0004970 | Ascending tubular aorta aneurysm | |
| HP:0006695 | Atrioventricular canal defect | |
| HP:0006689 | Bacterial endocarditis | |
| HP:0001647 | Bicuspid aortic valve | |
| HP:0001640 | Cardiomegaly | |
| HP:0100749 | Chest pain | |
| HP:0001680 | Coarctation of aorta | |
| HP:0001653 | Mitral regurgitation | |
| HP:0012764 | Orthopnea | |
| HP:0001962 | Palpitations | |
| HP:0004757 | Paroxysmal atrial fibrillation | |
| HP:0030973 | Postexertional malaise | |
| HP:0030950 | Pulmonary venous hypertension | |
| HP:0001642 | Pulmonic stenosis | |
| HP:0001279 | Syncope | |
Annotation source: 26538250[PMID]_30252341[PMID]_23947905[PMID]
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/3092
- This record as JSON: /data/d/3092.json