Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
Activity
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Disease of genetic or genomic mechanism
/
Hereditary disease
/
Bone Paget disease
Paget disease of bone 2, early-onset
rare
Identifiers
MONDO:0011183
OMIM:602080
Causal genes
TNFRSF11A
Part of
Bone Paget disease
Primary osteolysis
Also known as
PDB2
Projects
Sign in to start a project
No projects yet.