Global Variome shared LOVD

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Phenotype #0000045652 Individual ID 00059062 Associated disease HTX1 Phenotype details Two male fetuses with heterotaxy, one living male with heterotaxy and caudal regression syndrome Diagnosis/Initial - Inheritance Familial, X-linked recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Aimee Paulussen Database submission license No license selected Created by Aimee Paulussen Date created 2016-02-19 14:52:00 +01:00 (CET) Date last edited N/A

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