CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 3
OrphanetNr:
OMIM Id: 614954
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0005110) Atrial fibrillation 71 / 7739
2
(HPO:0005301) Persistent left superior vena cava 4 / 7739
3
(HPO:0001636) Tetralogy of Fallot 104 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: