Disease #01588 (ETM1 (tremor, essential hereditary, type 1 (ETM1)), OMIM:190300)

Global Variome shared LOVD

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Official abbreviation	ETM1
Name	tremor, essential hereditary, type 1 (ETM1)
OMIM ID	190300
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DRD3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-05-15 10:28:55 +02:00 (CEST)

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