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
/
Overgrowth syndrome
/
Beckwith-Wiedemann syndrome
Beckwith-Wiedemann syndrome due to CDKN1C mutation
rare
Identifiers
MONDO:0016476
Orphanet:231120
Part of
Beckwith-Wiedemann syndrome
Projects
Sign in to start a project
No projects yet.