Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
Activity
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Disorder of development or morphogenesis
/
Demyelinating disease
Boylan dew greco syndrome
rare
Identifiers
MONDO:0022025
Part of
Arthrogryposis
Demyelinating disease
Inherited neurodegenerative disorder
Also known as
congenital hypomyelination neuropathy with arthrogryposis multiplex congenita
Projects
Sign in to start a project
No projects yet.