Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Nervous system disorder
/
Hereditary neurological disease
/
Mendelian neurodevelopmental disorder
/
Genetic developmental and epileptic encephalopathy
Developmental and epileptic encephalopathy 98
rare
Identifiers
MONDO:0030472
OMIM:619605
Causal genes
ATP1A2
Part of
Genetic developmental and epileptic encephalopathy
Also known as
DEE98
Projects
Sign in to start a project
No projects yet.