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
03117 OPTB-7 osteopetrosis, autosomal recessive, type 7 (OPTB-7) 612301 - - - TNFRSF11A - -
01514 PDB-2 Paget disease of bone, type 2, early-onset (PDB-2, expansile osteolysis) 174810 - - - TNFRSF11A - -
02411 PDB-2 Paget disease of bone, type 2, early-onset (PDB-2) 602080 - - - SQSTM1, TNFRSF11A - -
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