Phenotype #0000257301

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	00361905
Associated disease	EPM3;CLN14
Phenotype details	Neuroregression, myoclonic epilepsy
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Anju Shukla
Database submission license	No license selected
Created by	Anju Shukla
Date created	2021-04-12 07:00:39 +02:00 (CEST)
Date last edited	2021-04-12 14:21:33 +02:00 (CEST)

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