Phenotype #0000087496

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00111411
Associated disease	BRWS1
Phenotype details	Severe ID, congenital heart defect, cleft lip and palate, epilepsy, behavioural anomalies, dysplastic ears, pre-auricular pit, downslanting palpebral fissures
Diagnosis/Initial	-
Inheritance	Isolated (sporadic)
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Bernt Popp
Database submission license	No license selected
Created by	Bernt Popp
Date created	2017-08-03 07:41:58 +02:00 (CEST)
Date last edited	2017-08-04 09:29:30 +02:00 (CEST)

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