juvenile absence epilepsy 1 Disease Ontology Browser

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Disease Ontology Browser

juvenile absence epilepsy 1 (DOID:0111324)
Alliance: disease page
Synonyms: EJA1; JAE1
Alt IDs: OMIM:607631
Definition: A juvenile absence epilepsy that has_material_basis_in heterozygous mutation in EFHC1 on 6p12.2.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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