Disease #05920 (NEDMIAL (neurodevelopmental disorder with severe motor impairment and absent language (NEDMIAL)), OMIM:617804)

Official abbreviation	NEDMIAL
Name	neurodevelopmental disorder with severe motor impairment and absent language (NEDMIAL)
OMIM ID	617804
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DHX30
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-04-09 08:40:02 +02:00 (CEST)
Date last edited	2021-04-09 08:40:27 +02:00 (CEST)

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Global Variome shared LOVD