Phenotype #0000201929

Individual ID 00264087
Associated disease CHD
Inheritance Familial, autosomal dominant
Diagnosis/Initial congenital heart disease
Age/Examination -
Diagnosis/Definite -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Phenotype details see paper; ..., familial history atrial septal defect (HP:0001631), thyroglossal sinus, refractive errors eye, mitral stenosis (HP:0001718)
Protein -
Owner name Ehsan Razmara
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-09-10 12:02:21 +02:00 (CEST)
Date last edited N/A

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