All diseases

9 entries on 1 page. Showing entries 1 - 9.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05306 BMND bone mineral density, quantitative trait locus (BMND) - - 11 11 PLS3, WNT1 - -
03856 BMND16 bone mineral density quantitative trait locus 16 (BMND-16) 615221 AR - - WNT1 - -
05296 OI osteogenesis imperfecta - - 4591 1414 BMP1, CCDC134, COL1A1, COL1A2, CREB3L1, CRTAP, FAM46A, FKBP10, IFITM5, KDELR2, KIF5B, MBTPS2, MESDC2, P3H1, PHLDB1, SERPINF1, SERPINH1, SP7, SPARC, TMEM38B, WNT1 - -
03855 OI15 osteogenesis imperfecta, type XV (OI15) 615220 AR 3 3 WNT1 - -
01979 OODD dysplasia, odontoonychodermal (OODD) 257980 AR - - WNT10A - -
01768 SHFM6 split-hand/foot malformation, type 6 (SHFM-6) 225300 AR 6 6 WNT10B - -
01762 SSPS Schopf-Schulz-Passarge syndrome (SSPS) 224750 AR 2 2 WNT10A - -
01411 STHAG4 agenesis, tooth, selective, type 4 (STHAG-4) 150400 AD;AR 1 1 WNT10A - -
05251 STHAG8 agenesis, tooth, selective, type 8 (STHAG-8) 617073 AD - - WNT10B - -
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