Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000227020 Individual ID 00299708 Associated disease PCKDC Phenotype details Severe LVOT obstruction LV hypertrophy. Recurrent sub-aortic membrane. Congenital heart valve disease. Diagnosis/Initial Congenital heart disease Inheritance Familial, autosomal recessive Diagnosis/Definite Congenital heart valve disease. Age/Examination - Age/Diagnosis 00y10m Age/Onset - Phenotype/Onset congenital Protein - Owner name Aida Bertoli-Avella Database submission license No license selected Created by Aida Bertoli-Avella Date created 2020-04-20 15:12:24 +02:00 (CEST) Date last edited 2020-04-21 09:47:57 +02:00 (CEST)

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