Disease #00832 (RESDX (epilepsy, Rolandic, mental retardation, and speech dyspraxia (RESDX)), OMIM:300643)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	RESDX
Name	epilepsy, Rolandic, mental retardation, and speech dyspraxia (RESDX)
OMIM ID	300643
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SRPX2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2017-08-11 13:01:14 +02:00 (CEST)

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