raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:3092

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enFixed subaortic stenosis
frRétrécissement aortique sous-valvulaire
deSubaortenstenose, fixierte
esEstenosis subaórtica fija
itStenosi subaortica fissa
nlGefixeerde subaortastenose
ptEstenose subaórtica fixa
plZwężenie podaortalne
csFixovaná subaortální stenóza
ukФіксований субаортальний стеноз
zh主动脉瓣下固定性狭窄
trSabit subaortik stenozu

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
OMIM271950BTNTvalidated
ICD-10Q24.4Especificvalidated
ICD-11LA8A.5NTBTindexvalidated
MONDO0017727Evalidated
UMLSC0265853Evalidated

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):

Children (3):

4

Genes

0 direct

Orphanet records no gene directly on this code.

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Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Point prevalenceUnknown—WorldwideClass onlyNot yet validatedORPHANET

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

28 annotations · validated 2021-08-19
HPOTerm (as annotated by Orphanet)Diagnostic
Frequent (79-30%)
HP:0001627Abnormal heart morphology
HP:0001659Aortic regurgitation
HP:0001635Congestive heart failure
HP:0031668Diastolic heart murmur
HP:0002094Dyspnea
HP:0002875Exertional dyspnea
HP:0001712Left ventricular hypertrophy
HP:0032092Left ventricular outflow tract obstruction
HP:0001643Patent ductus arteriosus
HP:0031664Systolic heart murmur
HP:0001629Ventricular septal defect
Occasional (29-5%)
HP:0001671Abnormal cardiac septum morphology
HP:0001681Angina pectoris
HP:0004970Ascending tubular aorta aneurysm
HP:0006695Atrioventricular canal defect
HP:0006689Bacterial endocarditis
HP:0001647Bicuspid aortic valve
HP:0001640Cardiomegaly
HP:0100749Chest pain
HP:0001680Coarctation of aorta
HP:0001653Mitral regurgitation
HP:0012764Orthopnea
HP:0001962Palpitations
HP:0004757Paroxysmal atrial fibrillation
HP:0030973Postexertional malaise
HP:0030950Pulmonary venous hypertension
HP:0001642Pulmonic stenosis
HP:0001279Syncope

Annotation source: 26538250[PMID]_30252341[PMID]_23947905[PMID]

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Sources for this card