Disease #05293 (EIEE37 (encephalopathy, epileptic, early infantile, type 37 (EIEE-37)), OMIM:616981)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	EIEE37
Name	encephalopathy, epileptic, early infantile, type 37 (EIEE-37)
OMIM ID	616981
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FRRS1L
Associated tissues	-
Disease features	-
Remarks	-
Date created	2017-06-24 22:05:29 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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