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Disease Ontology Browser
developmental and epileptic encephalopathy 79 (DOID:0112215)
Alliance: disease page
Synonyms: DEE79; early infantile epileptic encephalopathy 79
Alt IDs: OMIM:618559
Definition: A developmental and epileptic encephalopathy characterized by onset in the first months of life of refractory seizures, severely impaired psychomotor development, hypomyelination, cerebral atrophy, and thinning of the corpus callosum that has_material_basis_in heterozygous mutation in the GABRA5 gene on chromosome 15q12.

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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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11/12/2024
MGI 6.24 		The Jackson Laboratory