Phenotype #0000297299

Individual ID 00404724
Associated disease HTX
Phenotype details Dextrocardia, Aortic valve stenosis, Abnormal heart morphology, Sinus bradycardia, Ventricular septal defect, Echogenic fetal bowel, Increased nuchal translucency, Abnormality of prenatal development or birth, Heterotaxy
Diagnosis/Initial prental
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Date created 2022-03-07 13:14:13 +01:00 (CET)
Date last edited 2022-03-07 14:04:09 +01:00 (CET)

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