Phenotype #0000199673

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00261167
Associated disease	DD
Phenotype details	developmental delay/intellectual disability (HP:0012758/HP:0001249); apraxia
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	5y (5 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2019-08-11 12:19:47 +02:00 (CEST)
Date last edited	N/A

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