Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Disorder of development or morphogenesis
Hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome
rare
Identifiers
MONDO:0018655
Orphanet:447893
Part of
Disorder of development or morphogenesis
Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism
Projects
Sign in to start a project
No projects yet.