Phenotype #0000054269

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00074419
Associated disease	MPMCD
Phenotype details	congenital cataract (HP:0000519), slight axial hypotonia (HP:0000519)
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	03y (3 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Jamie Zeegers
Database submission license	No license selected
Created by	Johan den Dunnen
Date created	2016-07-02 11:19:20 +02:00 (CEST)
Date last edited	N/A

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