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Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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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
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