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DO Term : familial adult myoclonic epilepsy 6 [DOID:0111696] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A familial adult myoclonic epilepsy that has_material_basis_in a heterozygous 5-bp repeat expansion in the TNRC6A gene on chromosome 16p12.1.

synonyms:
FCMTE6,
familial cortical myoclonic tremor and epilepsy 6,
BAFME6,
benign adult familial myoclonic epilepsy 6,
OMIM:618074,
618074,
FAME6

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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