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
Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis
rare
Identifiers
MONDO:0014679
OMIM:616531
Part of
PI4KA-related disorder
Bilateral perisylvian polymicrogyria
Hereditary neurological disease
Also known as
PMGYCHA
Projects
Sign in to start a project
No projects yet.