All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01383 - hyperostosis, endosteal (Worth disease) 144750 - - - LRP5 - -
01484 - osteoporosis 166710 - - - CALCR, COL1A1, COL1A2, LRP5, PDLIM4, VDR - -
02685 - Van Buchem disease type 2 607636 - - - LRP5 - -
02399 BMND-1 bone mineral density quantitative trait locus 1 (BMND-1) 601884 - - - LRP5 - -
02391 EVR-4 vitreoretinopathy, exudative, type 4 (EVR-4) 601813 - - - LRP5 - -
00675 OPPG osteoporosis-pseudoglioma syndrome (OPPG) 259770 - - - LRP5 - -
02684 OPTA-1 osteopetrosis, autosomal dominant, type 1 (OPTA-1) 607634 - - - LRP5 - -
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