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
/
Joubert syndrome
Joubert syndrome 31
rare
Identifiers
MONDO:0033310
OMIM:617761
Causal genes
CEP120
Part of
Joubert syndrome
Also known as
JBTS31
Projects
Sign in to start a project
No projects yet.