Disease #07040 (NEDMILEG (neurodevelopmental disorder with microcephaly, impaired language, epilepsy, gait abnormalities, autosomal dominant), OMIM:619092)

Global Variome shared LOVD

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Official abbreviation	NEDMILEG
Name	neurodevelopmental disorder with microcephaly, impaired language, epilepsy, gait abnormalities, autosomal dominant
OMIM ID	619092
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NARS
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-11-09 09:26:21 +01:00 (CET)
Date last edited	N/A

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