Developmental and epileptic encephalopathy, 19

Developmental and epileptic encephalopathy, 19

Definition

Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the GABRA1 gene.

Also known as DEE19, developmental and epileptic encephalopathy 19, Early Infantile epileptic encephalopathy 19, early infantile epileptic encephalopathy caused by mutation in GABRA1, EIEE19, epileptic encephalopathy, early infantile, 19, epileptic encephalopathy, early infantile, type 19, GABRA1 early infantile epileptic encephalopathy — per MONDO

Also identified as

Affected Organs

Organ Involvement Source
Brain Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Brain Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Central nervous system Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Central nervous system Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Nervous system Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Nervous system Disease Has Primary Anatomic Site NCIT · CC BY 4.0