|
DOID:936 - brain disease
Disease Ontology Definition:A central nervous system disease that is located_in the brain.
Synonyms: encephalopathy,
Xenbase Genes : sufu, tnf, il6, pde6d, gnal, nos3, hoxa1, apc, f2, psen1, tubb, esr1, pparg, 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, pnkd, kif2a, ppp3ca, elovl5, taf1, prnp, abcd1, ca8, elovl4,
pex10, lgi1, grid2, uba5, ano10, rars1, cntnap2, atxn7, arl3, pum1, mre11, kcnc3, aimp1, atxn10, cpa6,
gch1, eif2b3, cep104, cplane1, atcay, 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, tnrc6a, atxn1, reln, slc6a3, slc19a3, guf1, gucy1a1, snx14,
prdm8, fxn, angptl6, tmem67, pex1, syt14, cilk1, eif2b5, dnm1, sptan1, mapt, f5, kctd7, ntn1, rubcn,
armc9, sacs, drd5, grin2a, wdr11, cacna1g, cstb, mpdz, scn1b, crh, cers1, cwf19l1, grn, atp1a3, piga,
kcnc1, tpp1, eif2b4, lztr1, aimp2, col6a3, adra2b, KIAA0753, nid1, idh1, drd2, trim8, ednra, mecr, med17,
neurod2, plp1, sptbn2, thap1, pex5, mapk10, polr1c, dab1, kcna1, nhlrc1, mme, efhc1, scn8a, ofd1, oprm1,
gad1.1, tmem231, ano3, cacnb4, polr3a, atg5, slc25a22, pex13, cacna1a, chrna2, 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, nprl3, slc6a1, gad1.2, rpgrip1l,
arl3l2, scyl1, tmem106b, pigq, kcnd3, gosr2, cep120, tgm6, ahi1, nop56, ccdc88a, tubb3, tctn1, cc2d2a, gal.2,
l1cam, add3, KIAA0586, erbb2, tmem216, gabrg2, col4a2, pnkp, syne1, 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, hepacam, rnf213, cntn2, samd12, cabp4, pdgfrb, aars2, wdr81,
scn2a, syn1, notch3, col4a1, brca2, cnpy3, atn1, sik1, cfap43, tctn3, hyls1, gabrb2
MONDO:0005560 - brain disorder |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
central nervous system disease (is_a)