Disease #03726 (ETM4 (tremor, hereditary essential, type 4 (ETM4)), OMIM:614782)

Official abbreviation ETM4
Name tremor, hereditary essential, type 4 (ETM4)
OMIM ID 614782
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene FUS
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-05-15 10:30:00 +02:00 (CEST)

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