Phenotype #0000300390

Individual ID 00408262
Associated disease HOS
Phenotype details atypical HOS family with early onset atrial fibrillation and heterogeneous clinical traits; HP:0000924 - Abnormality of the skeletal system; HP:0001627 - Abnormal heart morphology; HP:0005110 - Atrial fibrillation; HP:0011702 - Abnormal electrophysiology of sinoatrial node origin; HP:0001678 - Atrioventricular block; HP:0001631 - Atrial septal defect; HP:0001629 - Ventricular septal defect
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Alaaeldin Fayez
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Alaaeldin Fayez
Date created 2022-04-18 12:53:26 +02:00 (CEST)
Date last edited 2022-04-25 17:37:00 +02:00 (CEST)

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