Phenotype #0000349957

Individual ID 00462458
Associated disease HTX
Phenotype details see paper; ..., situs inversus; right-sided stomach, midline liver, right-sided spleen, cecum in the left-lower quadrant; dextrocardia, transposition great arteries, pulmonary atresia, patent ductus arteriosus, atrial septal defect, ventricular septal defect, left aortic arch, common origin right innominate and left common carotid arteries; subdural; subpial; subarachnoid hemorrhages; feeding intolerance; episodes of hypoglycemia and lactic acidosis
Diagnosis/Initial heterotaxy
Inheritance Familial, autosomal recessive
Diagnosis/Definite HTX14
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2025-02-10 14:19:55 +01:00 (CET)
Date last edited N/A

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