Phenotype #0000308050

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00416283
Associated disease	del 1p36
Diagnosis/Initial	1p36 deletion syndrome
Diagnosis/Definite	-
Phenotype details	developmental delay, ataxia, dyspraxia, wide-based gait; Brown syndrome, amblyopia
Inheritance	Isolated (sporadic)
Age/Examination	5y (5 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2022-08-26 10:31:45 +02:00 (CEST)
Date last edited	N/A

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