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DOID:936 - brain disease
Disease Ontology Definition:A central nervous system disease that is located_in the brain.
Synonyms: encephalopathy
Xenbase Genes : sufu, atp6v1a, tnf, il6, pde6d, gnal, nos3, hoxa1, apc, f2, psen1, tubb, esr1, pparg, slc12a5, [+]
fgf14, arx, tp53, slc9a1, nkx2-1, nphp1, prkch, prickle1, ctnnb1, cux2, pdgfb, htra1, ptch1, tbp, lmnb1,
ifrd1, lmnb2, tubb2b, tubg1, pten, hpca, aldh7a1, alox5ap, kcnq3, ttbk2, smarcb1, atm, acta2, clcn2, mecp2,
sgce, ndufv1, fus, dcc, chrnb2, nprl2, hycc1, dnal4, prkcg, kank1, gal.1, atxn2, itpr1, gnao1, kcnma1,
vps11, ntrk2, vps13d, slc18a2, prkra, st3gal3, me2, tor1a, rnaset2, afg3l2, stxbp1, ppp2r2b, tubb4a, pigp, scarb2,
chmp2b, pibf1, grin2b, plpbp, hcn1, tdp1, chd2, cdkl5, ywhag, pnkd, kif2a, ppp3ca, elovl5, taf1, prnp,
abcd1, ca8, elovl4, pex10, lgi1, grid2, uba5, ano10, rars1, cntnap2, atxn7, synj1, arl3, adam22, pum1,
mre11, kcnc3, aimp1, atxn10, cpa6, gch1, eif2b3, cep104, cplane1, atcay, rhobtb2, atp6ap2, dnmt1, epm2a, stub1,
eprs1, setx, tdp2, hikeshi, xrcc1, gjc2, eef2.1, pex26, b9d1, atxn3, vldlr, wdr45, eif2b1, pcna, ufm1,
tmem138, eif2b2, mlc1, pmpca, kif5c, msh2, spr, scn1a, hspd1, grm1, arhgef9, cep41, depdc5, tbc1d24, tnrc6a,
atxn1, reln, slc6a3, kcnb1, slc19a3, guf1, gucy1a1, slc13a5, snx14, prdm8, fxn, angptl6, tmem67, pex1, syt14,
cilk1, eif2b5, dnm1, sptan1, mapt, f5, kctd7, ntn1, rubcn, armc9, kcna2, sacs, drd5, grin2a, wdr11,
cacna1g, cstb, mpdz, scn1b, crh, cers1, cwf19l1, grn, atp1a3, piga, necap1, kcnc1, tpp1, eif2b4, dock7,
lztr1, aimp2, col6a3, adra2b, KIAA0753, itpa, slc25a12, nid1, idh1, slc1a2, drd2, trim8, ednra, mecr, med17,
neurod2, plp1, sptbn2, thap1, pex5, mapk10, polr1c, adgrv1, pdcd10, dab1, kcna1, nhlrc1, mme, efhc1, scn8a,
ofd1, oprm1, gad1.1, tmem231, ano3, cacnb4, polr3a, atg5, slc25a22, ap3b2, pex13, cacna1a, chrna2, ccm2, tenm4,
trpc3, braf, arl13b, cask, slc20a2, aptx, tctn2, tmem237, xpr1, pik3r5, aspa, rad51, fgfr1, ccdc88c, ptch2,
pcdh19, mks1, cep290, wwox, znhit3, pdyn, slc2a1, l2hgdh, cspp1, eef2.2, fam149b1, abr, polr3b, scn3a, rapgef2,
gabbr2, cplx1, nprl3, slc6a1, gad1.2, rpgrip1l, arl3l2, scyl1, tmem106b, pigq, kcnd3, gosr2, cep120, tgm6, cad,
ahi1, nop56, ccdc88a, tubb3, tctn1, pacs2, cc2d2a, gal.2, l1cam, add3, KIAA0586, erbb2, tmem216, gabrg2, col4a2,
pnkp, syne1, tbc1d24.2, phactr1, stx1b, kcnt1, chrna4, plekhg4, dmbt1, gabrb3, inpp5el, prrt2, cacna1b, tmem240, gabra1,
atp1a2, kif7, kctd17, atp8a2, kras, szt2, vwa3b, adgrg1, cacna1h, camta1, fat2, plcb1, fig4, kcnq2, myorg,
ttc21b, gabrb1, hepacam, rnf213, cntn2, samd12, cabp4, pdgfrb, aars2, wdr81, scn2a, syn1, notch3, col4a1, brca2,
cnpy3, atn1, sik1, cfap43, tctn3, hyls1, gabrb2, alg13
MONDO:0005560 - brain disorder |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
central nervous system disease (is_a)