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Start free with EleplanAtrial septal defect, coronary sinus type
ORPHA:99104Clinical subtype
Also called ASD, coronary sinus type · Unroofed coronary sinus
What it is
Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.
Key facts
- Age of onset
- Antenatal, Infancy, Neonatal
- Classified as
- Clinical subtype
Recorded for the broader condition
- Prevalence
- 1-5 / 10 000Interatrial communication
- Inheritance
- Autosomal dominant, Not applicableInteratrial communication
Orphanet records these for the broader condition rather than for this specific form. They are a starting point, not a figure for this subtype — subtypes often differ, and some are defined by being rarer than the condition they sit under.
Signs and symptoms
Common30–79%
8Sometimes5–29%
9- Arrhythmia
- Bundle branch block
- Dyspnea
- Presyncope
- Pulmonary arterial hypertension
- Right atrial enlargement
- Right ventricular dilatation
- Supraventricular arrhythmia
and 1 more in this range
These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.
ICD-10 codes
ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.
Related health topics
Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.
Cross-references
Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.
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