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DOID:17 - musculoskeletal system disease
Disease Ontology Definition:A disease of anatomical entity that occurs in the muscular and/or skeletal system.
Synonyms:
Xenbase Genes

gjb1, smad6, map3k7, tnnt1, tnfsf11, gdf5, zfpm2, bmp2, tnxb, runx2, tnfrsf11a, hoxd13, foxo1, tnnt3, wnt10b,
pax3, ncf2, fgf23.2, ctla4, pparg, runx1, mstn, bmpr1b, rab7a, fgf16, ihh, popdc1, tp53, ca2, fn1,
fgf9, atp1a1, gli3, mmp1, lrp5, hoxd10, wnt1, pitx1, lemd3, mybpc1, hes7.2, vdr, pax7, gdf3, mif,
pdgfb, nog, lfng, tgfb1, aspscr1, sh3tc2, tbce, creb3l1, itga6, cav1, rab33b, pten, ror2, yars1, cntn1,
acta1, megf10, nefl, ppp1r3a, adamts2, syne2, rab23, sf3b4, col1a2, nfkbil1, smarcal1, fgd4, nr4a3, flnc, gfpt1,
ski, p4hb, lrp4, alg2, fbn2, flnb, des, hnrnpdl, sftpc, dmd.2, erf, msx2, fbxw4, dlx5, dlx6,
egr2, erbb3, ptpn22, dync1h1, prdm5, mstn.2, cox6a1, ppib, prkar1a, ext1, ext2, hes7, myo18b, gja1, col11a2,
smad6.2, mpz, chd7, cnbp, des.2, wdr19, nefh, fgf23, lmna, shox, acan, ldb3, gmppb, musk, tnfrsf11b,
hcn4, slc34a3, evc2, antxr2, agpat2, snx10, trim2, cyp27b1, ncf4, sgcb, kars1, pomt1, hk1, serpinf1, hspb8,
mhc2-dcb, tgds, stim1, snap25, xylt1, plin1, sgcd, dmpk, slc2a10, por, tbx4, dnajb2, calcr, bank1, dpagt1,
dync2i2, micu1, mbtps2, lama2, agrn, fbn1, zmpste24, sp7, neb, tor1aip1, jph1, lgi1, emd, plod1, myot,
ripply2, sgcg, bscl2, pth1r, pthlh, dnm2, cyba, eps15l1, yars2, pomgnt1, tfg, slc5a7, tmem43, orai1, cav3,
gars1, aars1, pus1, fhl1, fkrp, cidec, pdk3, slc18a3, mccc1, ccn6, atp2c1, smchd1, klhl40, bag3, vcp,
cfap410, znf687, rrm2b, gnb4, cryab, mtap, fktn, dnajb6, gle1, ap1s3, b4galt7, pomgnt2, b3galt6, atp2a1, cant1,
samhd1, chrna1, msh2, nans, cybc1, gdap1, cybb, twnk, chrne, bin1, kif22, dhtkd1, syt2, dync2li1, lmbr1,
scn4a, nek1, lamb3, syne2.2, ddr2, taf15, chat, pomk, lama3, faslg, zswim6, matn3, wdr35, itga7, map3k20,
mccc2, ky, papss2, enpp1, lipe, mypn, myh3, p3h1, itgbl1, ostm1, card14, ecel1, chrnd, lamc2, gpx4,
ifitm5, ift81, rapsn, kbtbd13, slc35d1, myh7l, evc, ciita, npr2, ndrg1, chst3, wdr11, xylt2, comp, lrsam1,
clcn7, c1r, c1s, cavin1, slc39a13, inpp5k, slc26a2, col9a3, recql4, myf6, lztr1, tnpo3, col6a3, col6a1, elmod2,
trpv4, ncf1, pcyt1a, slc25a4, morc2, pdlim4, mtm1, dst, dnase1l3, cfl2, bgn, sec24d, top3a, gne, megf8,
sbf2, pmp22, idh1, serpinh1, polr1a, piezo2, dguok, col9a2, prx, pomt2, pabpn1, fkbp10, b4gat1, prps1, frg1,
sh3pxd2b, rxylt1, sparc, crtap, polg2, ankh, mme, ankrd11, ddit3, rnaseh1, trim32, b3galnt2, phex, col12a1, pde4d,
dse, ryr1, sbf1, kif1b, itgb4, tcap, inppl1a, cyp2r1, braf, ift80, crppa, mipol1, dag1, sem1, aifm1,
litaf, rb1, fgfr2, fgfr1, lpin1, sox9, slc26a2.2, ift140, ift172, tcirg1, dym, vma21, lmod3, bpnt2, casq1,
mtmr14, myh2, fbln1, dync2h1, chek2, tcf12, slc25a46, dmd.3, dmd, cav3.2, pip5k1c, dna2, med25, dnase1, tent5a,
tmem38b, ufsp2, klhl41, slc22a4, inf2, col3a1, spg11, mt-co1, cep120, capn3, ctsk, ddr2l, ccdc78, wnt7a, stac3,
ift43, kcnj8, sqstm1, KIAA0586, trappc11, chrna1.2, trip11, erbb2, mhc1-uaa, tonsl, mars1, ano5, chkb, myh8, col5a1,
syne1, clcn5, chchd10, dmbt1, naglu, ttn, col5a2, plekhm1, colq, traf3ip2, scn5a, dok7, gpc6, plekhg5, mtmr2,
muc5b, flna, itgam, tpm3, padi4, notch2, fig4, adamtsl2, ttc21b, col9a1, dync2i1, ltbp3, ptpn11, tpm2, abcc9,
dysf, col6a2, cog4, clcn1, pdgfrb, large1, tbx6, hmga2, ighmbp2, col2a1, sgca, col1a1, ewsr1, chrnb1, pcnt,
notch3, tert, col4a1, slc22a18, surf1, gdf6, pam16, selenon, poglut1, znf469, dmp1, plec, pop1, mt-cyb, col13a1,
hspg2, abcc6, mt-nd1, mesp2, col17a1, sftpa1, col10a1, mt-co3, mt-nd5, mt-nd4, mt-nd6, ripply2.2, mmp13, col11a1, kras,
amer1, col7a1, sftpa2
MONDO:0002081 - cardiac atrium |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
disease of anatomical entity (is_a)