Disease #05744 (ETM6 (tremor, hereditary essential, type 6 (ETM6)), OMIM:618866)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	ETM6
Name	tremor, hereditary essential, type 6 (ETM6)
OMIM ID	618866
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NOTCH2NLC
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-05-15 10:26:04 +02:00 (CEST)
Date last edited	2020-05-15 11:00:32 +02:00 (CEST)

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