Phenotype #0000308480

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00416969
Associated disease	EVR2
Phenotype details	no hearing impairment; additional disease - glucose-6-phosphate dehydrogenase deficiency
Diagnosis/Initial	-
Inheritance	Familial, X-linked
Diagnosis/Definite	persistent fetal vasculature syndrome
Age/Examination	-
Age/Diagnosis	-
Age/Onset	3m
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2022-09-12 11:14:36 +02:00 (CEST)
Date last edited	N/A

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