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 cerebral atrophy and variable facial dysmorphism
rare
Identifiers
MONDO:0030999
OMIM:619244
Causal genes
TTC5
Part of
Mendelian neurodevelopmental disorder
Also known as
NEDCAFD
Projects
Sign in to start a project
No projects yet.