Global Variome shared LOVD

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Phenotype #0000001387 Individual ID 00002408 Associated disease SLOS Inheritance Unknown Diagnosis/Initial - Diagnosis/Definite - Age/Onset - Age/Examination - Phenotype/Onset - Phenotype details intrauterine death, autopsy diagnosis; multiple congenital anomalies, low estriol level in triplet test, typical dysmorphic features and spectrum of congenital anomalies Biochem - Protein - Severity_score - Age/Diagnosis - Owner name Division of Human Genetics, Innsbruck Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Division of Human Genetics, Innsbruck Date created 2013-03-26 10:51:32 +01:00 (CET) Date last edited N/A

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