Disease #05745 (ETM5 (tremor, essential hereditary, type 5 (ETM5)), OMIM:616736)

Official abbreviation ETM5
Name tremor, essential hereditary, type 5 (ETM5)
OMIM ID 616736
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ODZ4
Associated tissues -
Disease features -
Remarks -
Date created 2020-05-15 10:34:12 +02:00 (CEST)
Date last edited N/A

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