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DOID:0080006 - bone development disease
Disease Ontology Definition:A bone disease that results_in abnormal growth and development located_in bone or located_in cartilage.
Synonyms:
Xenbase Genes
:
sfrp4,
bmp1,
fgfr3,
twist1,
tp63,
apc,
smad6,
map3k7,
gdf5,
bmp2,
runx2,
hoxd13,
wnt10b,
bmpr1b,
fgf16,
[+]
ihh, fn1, fgf9, gli3, wnt1, pitx1, hes7.2, vdr, nog, lfng, tbce, creb3l1, rab33b, ror2, rab23,
sf3b4, col1a2, smarcal1, ski, p4hb, lrp4, flnb, erf, msx2, fbxw4, dlx5, dlx6, ppib, prkar1a, hes7,
gja1, col11a2, smad6.2, wdr19, lmna, shox, acan, evc2, cyp27b1, serpinf1, xylt1, por, tbx4, dync2i2, mbtps2,
fbn1, zmpste24, sp7, ripply2, pth1r, pthlh, eps15l1, ccn6, cfap410, mtap, b3galt6, cant1, nans, kif22, dync2li1,
lmbr1, nek1, ddr2, zswim6, matn3, wdr35, papss2, myh3, p3h1, gpx4, ifitm5, ift81, slc35d1, evc, npr2,
chst3, comp, slc26a2, col9a3, recql4, trpv4, pcyt1a, bgn, sec24d, megf8, serpinh1, polr1a, col9a2, fkbp10, sh3pxd2b,
sparc, crtap, pde4d, inppl1a, cyp2r1, ift80, mipol1, sem1, fgfr2, fgfr1, sox9, slc26a2.2, ift140, ift172, dym,
bpnt2, fbln1, dync2h1, tcf12, tent5a, tmem38b, ufsp2, cep120, ctsk, ddr2l, wnt7a, ift43, kcnj8, KIAA0586, trip11,
tonsl, ano5, gpc6, flna, adamtsl2, ttc21b, col9a1, dync2i1, ltbp3, ptpn11, abcc9, cog4, tbx6, col2a1, col1a1,
pcnt, gdf6, pam16, pop1, hspg2, mesp2, col10a1, ripply2.2, mmp13, col11a1
| MONDO:0005497 - non-neural ectoderm |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s):
bone disease (is_a)