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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:
Echinobase Genes
:
zeb2,
nf1,
rsph1,
wrn,
lrmda,
ret,
mttp,
pax2,
fras1,
pcdh15,
herc2,
ahi1,
ube3a,
ofd1,
fat4,
[+]
nsdhl, LOC105444109, ddx11, rnaseh2b, myo7a, ccdc39, bcs1l, cep63, cspp1, eya1, tfap2a, dnai2, dnaaf5, ercc6, nog,
abcc6, smc3, nsd1, LOC581500, fgfr3, hpse2, rnaseh2a, hps1, msx1, MMP14, sufu, eif2ak3, sil1, kif11, nphp4,
slc45a2, pde6d, hspg2, dcaf17, cep290, tmem138, aaas, eftud2, pms1, rab18, emg1, gle1, mks1, sbds, tbx1,
snap29, trim37, smarcb1, lztr1, b3glct, por, rogdi, efnb1, rbpj, shoc2, dnaaf3, cfap298, cep57, pex7, rpgr,
arl13b, mlh1, arl6, msh2, ercc4, cplane1, orc1, clpp, ptch1, ercc8, tsc1, lmx1b, whrn, rsph9, bbs1,
ush2a, LOC754546, rnaseh2c, wdr81, ercc2, polh, vipas39, banf1, tbce, six1, lyst, nphp1, LOC100891460, sdccag8, gnpat,
dnal1, gli3, epg5, cep152, kifbp, iqcb1, cep41, eogt, ebp, tubgcp6, zmynd10, hint1, agps, rbpj, porcn,
col2a1, smc1a, kansl1, ift122, tgfbr2, wdr35, drc1, armc4, spag1, rad21, dna2, ccdc103, rab3gap1, cdc6, tmem67,
rpgrip1l, pign, pigt, ca8, slc52a3.2, slc52a3, recql4, lars2, nbn, tbc1d20, tmem231, hpgd, sall1, cdt1, orc6,
dnah5, vps33b, dnai1, dnajc21, ttc37, xpa, blm, ddx59, adgrv1
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
disease (is_a)