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DOID:225 - syndrome
Disease Ontology Definition:A disease characterized by a group of signs and symptoms that occur together and characterize a particular abnormality.
Synonyms:
Xenbase Genes

notch1, hras, bcap31, zeb2, wnt3, tp63, hoxa13, nr2f1, sox10, zic3, tgfb2, six1, sox4, rasa2, apc,
dll4, rps6ka3, tfap2a, foxc2, ghr, kremen1, gdf5, gli2, smad3, slc4a11, cdh3, ep300, hoxd13, smarce1, igf2,
gli1, zic2, pax3, mmp2, spred1, bmp4, hesx1, sox18, sox11, cdh11, dvl1, arx, smarca4, pax6, wnt4,
tp53, sox2, ahsg, sox3, gli3, tp53rk, akt1, mitf, wt1, fgf10, gata6, kmt2c, lrp5, ret, otx2,
sall4, zfhx2, tgfbr2, bmpr1a, mmp14, smad4, lemd3, lrp2, skic2, nphp1, fst, mybpc1, foxl2, pax2, tbx5,
dnm1l, gdf3, arnt2, nphp4.2, meis2, nog, nphp3, nf1, shh, tgfb1, ifng, ptch1, zbtb24, tbce, mras,
rab18, krt17, msx1, prokr2, tubgcp6, brca1, smarcc2, rbpj, actb, hnrnpa2b1, nfkbia, tubb2b, sall1, pten, eed,
ror2, actg1, tubgcp4, arid1a, smarcad1, shoc2, rab39b, smarcb1, plk4, atrip, hnrnpa1, myo7a, foxi1, clcf1, ripk4,
mid1, flnb, mecp2, lmx1b.1, ndp, alx4, grip1, tgif1, alx1, nipbl, erbb3, vps13b, slc24a5, ocln, cftr,
hps3, adar, hps6, kmt2d, prkar1a, ext1, irf6, myo18b, gja1, col11a2, tgfbr2l, chd7, grhl3, intu, mnx1,
rbm28, wdr19, lmx1b.2, lmna, insr, itpr1, men1, porcn, bbs2, trem2, traip, crlf1, cdon, lrig2, sema3e,
musk, mylkl, mlxipl, ctsc, arl6, evc2, chrm3, scarf2, sgo1, snap29, hps4, atp6v1b2, hpgd, mplkip, aldh3a2,
osgep, nbn, dpf2, edar, colec10, rnaseh2a, brf1, rspo2, slc45a2, gnas, gnpat, ube3a, ercc2, slc26a4.3, gorab,
hccs, por, b3glct, kcnk9, bbs4, cenpe, yap1, colec11, cep63, slc19a2, sdccag8, mbtps2, ca8, fbn1, nin,
zmpste24, bbs9, lrmda, st3gal5, gjb2, lars2, ezh2, cnnm4, ush2a, ccdc28b, pth1r, smc3, cdh23, bloc1s6, rogdi,
emg1, pnpla6, pms1, kdm6a, ercc5, pign, pstpip1, agps, wipf1, atp6v0a2, srp54, ppp1cb, adamts10, chsy1, gtf2e2,
ebf3, nsun2, pigl, tbc1d20, orc6, ednrb, fhl1, lig4, bbs5, naa10, sema3a, rhbdf2, ift122, gmnn, aaas,
dhodh, bbs10, clpp, vcp, ddx11, sdhb, klhl7, ddb2, vldlr, lars1, gle1, smc1a, eftud2, rps23, far1,
sec23b, cdc6, lztfl1, sdhc, iqcb1, vac14, mkks, cdc45, ddx59, idh2, gpc4, samhd1, fmr1, chrna1, cdca7,
dvl3, msh2, gnb5, hps1, xpa, sumo1, wfs1, twnk, kif11, bbs1, ikbkg, lmod1, ccdc22, atrx, slc16a2,
lep, slitrk6, fat4, vps33b, prepl, dync2li1, tbc1d24, tsc2, lmbr1, gpc3, rpgr, ift52, blm, pcsk1, edaradd,
nt5e, gmppa, masp1, nf2, trim37, tmem67, wdr35, znf592, cib2, srd5a3, cilk1, med12, nectin1, antxr1, msh6,
epcam, pcdh15, ercc4, cep57, ap3b1, rab3gap2, tsc1, alms1, tyr, cep152, opa1, smoc1, nsd1, oca2, myh3,
hpse2, whrn, crb2, copa, eif2ak3, chrnd, chrng, abhd12, rapsn, cacna1c, xpc, ocrl, ammecr1, vipas39, evc,
dock6, nfix, wrn, chst3, tbxas1, tbx22, eogt, apc2, setd2, rab3gap1, bbs7, inpp5k, ywhae, polh, piga,
suz12, recql4, orc1, pik3ca, lztr1, cox7b, pms2, slc3a1, nup133, sec23a, ttc8, ercc8, pola1, mtr, polr1d.1,
tyrp1, ift27, nxn, pafah1b1, bgn, sbds, txnl4a, frem2, rnaseh2b, nsdhl, idh1, mthfr, sos2, plod2, nup107,
ednra, fkbp10, ercc6, dnajc21, rad21, ap1s1, pex5, ercc3, polr1c, myt1, adgrv1, b3gat3, emc1, alpl, arid1b,
nfia, hsd17b4, bub1b, ifih1, ankrd11, ofd1, sos1, pole, tcf4, hhat, mttp, efnb1, fan1, tmem231, trim32,
lyst, orc4, herc2, nalcn, atr, cenpj, lonp1, ush1g, trps1, braf, gtf2h5, hint1, bloc1s3, cask, pigt,
ift80, cdt1, rad51d, bcs1l, ift74, rad51c, kdf1, pex7, flvcr2, tbx3, fgfr2, mc1r, ush1c, fgfr1, ptch2,
foxh1, gtf2i, pbx1, invs, ift172, mks1, cep290, slc19a3.2, mttp.2, banf1, tprkb, was, kansl1, dync2h1, rnf168,
chek2, rit1, kcnj10, washc5, ehmt1, c7h12orf57, rap1a, wdr73, dtnbp1, wdpcp, satb2, pip5k1c, tbc1d20.2, dna2, rpgrip1l,
mlh1, setd5, sprtn, polr1d.2, sdhd, gtf2ird1, asxl3, hdac8, bbip1, traf3ip1, nhs, snrpb, twist2, dlx3, hells,
cep78, lage3, eral1, ctnnd2, ercc1, sil1, rras2, wnt7a, bltp1, cc2d2a, ift43, chuk, nlrp3, irf6.2, stat5b,
epg5, kcnq1, ccnq, skic3, hps5, trappc11, chrna1.2, dctn1, kifbp, lamb2, specc1l, hars2, slc29a3, a2ml1, obsl1,
rbbp8, myh8, esco2, tbc1d24.2, dis3l2, mkrn3, bbs12, cisd2, smad10, slc52a3, mymk, pde3a, kif7, cep164, atp8a2,
srcap, kras, scn5a, dok7, cdk13, col4a5, dcaf17, clrn1, flna, fig4, arsl, dchs1, pdzd7, ltbp3, hepacam,
aggf1, ubr1, maf, raf1, ptpn11, pik3r1, arid2, hars1, ubb, kctd1, rnf113a, mafb, nras, rbm8a, wdr81,
col2a1, crebbp, wac, hmx1, notch3, fgd1, brca2, edn3, gdf6, plg, ebp, ptdss1, wdr4, tmem107, nsmce2,
prg4, wnt5a, sp110, plec, myh11, adamts17, rnaseh2c, eda, cfap418, hspg2, abcc6, arhgap31, arsg, tyrobp, tcof1,
cdkn1b, ckap2l, tctn3, hyls1, slc26a4.1, slc26a4.2, col11a1, cdkn1c, krt6b, mylk
MONDO:0002254 - syndromic disease |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
disease (is_a)