Phenotype #0000045652

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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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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