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DOID:331 - central nervous system disease
Disease Ontology Definition:A nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system.
Synonyms:
Xenbase Genes : app, sufu, ar, ace, tnf, il6, paxip1, pde6d, hspb1, gnal, nos3, hoxa1, apc, nr4a2, f2, [+]
a2m, fgf20, psen1, tubb, esr1, mpo, pparg, fgf14, arx, tp53, slc9a1, nkx2-1, nphp1, prkch, trpm7,
prickle1, ctnnb1, cux2, pdgfb, htra1, ptch1, tbp, smn1, lmnb1, ifrd1, lmnb2, tubb2b, tubg1, pten, pon2,
apbb2, hpca, aldh7a1, alox5ap, kcnq3, ttbk2, smarcb1, atm, prph, acta2, hnrnpa1, asah1, rax2, clcn2, mecp2,
sgce, ndufv1, fus, flrt1, dcc, apoe, chrnb2, dync1h1, nprl2, hycc1, dnal4, psen2, mn1, prkcg, kank1,
gal.1, erbb4, nefh, atxn2, pla2g6, itpr1, gnao1, kcnma1, vps11, als2, ntrk2, vps13d, slc18a2, reep1, prkra,
st3gal3, vps35, rtn2, ap4s1, me2, optn, tor1a, rnaset2, afg3l2, fars2, entpd1, stxbp1, adam10, hspb8, atl1,
ppp2r2b, tubb4a, btbd9, pigp, spast, scarb2, serpini1, sncaip, chmp2b, pibf1, ap4b1, grin2b, plpbp, erlin2, hcn1,
tdp1, chd2, cdkl5, pnkd, dnajb2, kif2a, ppp3ca, elovl5, taf1, prnp, abcd1, ca8, elovl4, pex10, wars1,
lgi1, grid2, tbk1, uba5, ano10, rars1, cntnap2, atxn7, synj1, bscl2, arl3, pum1, mre11, kcnc3, aimp1,
mtpap, anxa11, pnpla6, dbh, atxn10, kif1a, b4galnt1, tfg, slc12a6, cpa6, reep2, ddhd1, gch1, nipa1, eif2b3,
cep104, slc5a7, cplane1, exosc8, sepsecs, atcay, ndufv2, gars1, ccnf, ddhd2, atp6ap2, dnmt1, epm2a, ubtf, stub1,
eprs1, setx, exosc3, tdp2, hikeshi, irf2bpl, xrcc1, gjc2, fbxo38, tsen54, vps37a, hspb3, vcp, eef2.1, pex26,
ap4m1, cfap410, b9d1, dstyk, atxn3, slc33a1, vldlr, wdr45, eif2b1, pcna, gle1, ufm1, sncb, tmem138, eif2b2,
tardbp, slc1a3, dnajc6, dao, mlc1, arl6ip1, rars2, fmr1, pmpca, kif5c, msh2, atp2b3, spr, scn1a, spg21,
hspd1, grm1, toe1, arhgef9, cep41, depdc5, tnrc6a, atxn1, ampd2, reln, slc6a3, nek1, slc19a3, guf1, gucy1a1,
matr3, kif5a, tsen15, snx14, prdm8, fxn, nf2, angptl6, tmem67, pex1, syt14, cilk1, eif2b5, dnm1, sptan1,
mapt, f5, kctd7, jph3, ap4e1, pank2, nt5c2, ntn1, vps13a, rubcn, armc9, capn1, drd4, spart, sacs,
drd5, grin2a, exosc9, iba57, wdr11, cacna1g, cstb, mpdz, fbxo7, scn1b, crh, cers1, pde8b, cwf19l1, grn,
sorl1, bicd2l, atp1a3, coasy, piga, atp13a2, kcnc1, kif1c, blmh, tpp1, eif2b4, lztr1, aimp2, col6a3, trpv4,
adra2b, uchl1, KIAA0753, aco2, nid1, vrk1, idh1, zfyve26, slc1a2, park7, xk, drd2, sod1, trim8, pld3,
ednra, cyp2u1, mecr, med17, neurod2, plp1, sptbn2, thap1, clp1, pex5, c4h19orf12, mapk10, polr1c, pdcd10, dab1,
atp7a, kcna1, nhlrc1, mme, efhc1, scn8a, ofd1, oprm1, vps53, gad1.1, tmem231, zfyve27, ano3, cacnb4, polr3a,
atg5, slc25a22, htt, pex13, cacna1a, chrna2, ccm2, tenm4, trpc3, snca, braf, fa2h, arl13b, cask, slc20a2,
aptx, tctn2, tmem237, xpr1, pik3r5, aspa, rad51, fgfr1, ccdc88c, ptch2, pcdh19, ubtf.2, mks1, cep290, wwox,
pfn1, znhit3, bicd2, pdyn, slc2a1, l2hgdh, aldh18a1, lrrk2, cspp1, eef2.2, fam149b1, washc5, sigmar1, rnf170, erlin1,
abr, gba2, polr3b, scn3a, chmp1a, rapgef2, nprl3, slc6a1, tecpr2, gad1.2, rpgrip1l, arl3l2, scyl1, tmem106b, mars2,
pigq, kcnd3, spg11, gosr2, vamp1, c1h9orf72, cep120, uba1, tgm6, ahi1, nop56, ccdc88a, tubb3, tctn1, tbc1d23,
cyp7b1, tsen2, cc2d2a, gal.2, l1cam, dnajc13, sqstm1, add3, KIAA0586, tsen34, dctn1, erbb2, tmem216, gabrg2, col4a2,
pnkp, syne1, phactr1, chchd10, stx1b, kcnt1, chrna4, plekhg4, dmbt1, gabrb3, inpp5el, prrt2, cacna1b, slc52a3, tmem240,
gabra1, spg7, atp1a2, ap5z1, kif7, kctd17, atp8a2, kras, plekhg5, pclo, adh1c, szt2, vwa3b, adgrg1, cacna1h,
camta1, vps13c, fat2, plcb1, fig4, kcnq2, myorg, ttc21b, hepacam, rnf213, cntn2, samd12, cabp4, pdgfrb, aars2,
nup62, wdr81, ighmbp2, vapb, scn2a, syn1, notch3, col4a1, brca2, cnpy3, gba1, atn1, sik1, mag, cfap43,
mtrfr, tctn3, hyls1, gabrb2, podxl, jph3.2
MONDO:0002602 - central nervous system disorder |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
nervous system disease (is_a)