Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
Activity
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Nervous system disorder
/
Hereditary neurological disease
/
Mendelian neurodevelopmental disorder
Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language
Identifiers
MONDO:0976263
OMIM:621150
Causal genes
EEF1D
Part of
Mendelian neurodevelopmental disorder
Projects
Sign in to start a project
No projects yet.