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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
/
Hereditary disease
/
Familial osteosclerosis
/
Osteopetrosis
Osteosclerotic metaphyseal dysplasia
rare
Identifiers
MONDO:0014080
OMIM:615198
Orphanet:500548
Causal genes
LRRK1
Part of
Osteopetrosis
Also known as
OSMD
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