Disease #05556 (NEIMY (myoclonus, intractable, neonatal (NEIMY)), OMIM:617235)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	NEIMY
Name	myoclonus, intractable, neonatal (NEIMY)
OMIM ID	617235
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KIF5A
Associated tissues	-
Disease features	autosomal dominant
Remarks	-
Date created	2019-02-04 17:02:51 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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