Disease #06891 (NEDLIB (neurodevelopmental disorder with language impairment and behavioral abnormalities), OMIM:618917)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	NEDLIB
Name	neurodevelopmental disorder with language impairment and behavioral abnormalities
OMIM ID	618917
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GRIA2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-01-17 11:56:27 +01:00 (CET)
Date last edited	N/A

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