All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01514 FEO osteolysis, familial expansile (FEO, McCabe disease) 174810 AD - - TNFRSF11A - -
03117 OPTB7 osteopetrosis, autosomal recessive, type 7 (OPTB-7) 612301 AR 1 - TNFRSF11A - -
02411 PDB2 Paget disease of bone, type 2, early-onset (PDB-2) 602080 AD - - TNFRSF11A - -
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