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DOID:1289 - neurodegenerative disease
Disease Ontology Definition:A central nervous system disease that results in the progressive deterioration of function or structure of neurons.
Synonyms: degenerative disease, Neurodegenerative disease
Xenbase Genes

smn1, ifrd1, tubb2b, pon2, apbb2, ttbk2, atm, prph, hnrnpa1, asah1, rax2, fus, flrt1, apoe, dync1h1,
psen2, prkcg, erbb4, nefh, atxn2, pla2g6, itpr1, als2, vps13d, reep1, vps35, optn, afg3l2, adam10, hspb8,
ppp2r2b, serpini1, sncaip, chmp2b, tdp1, dnajb2, elovl5, ca8, elovl4, wars1, grid2, tbk1, uba5, ano10, atxn7,
synj1, bscl2, pum1, mre11, kcnc3, mtpap, anxa11, dbh, atxn10, slc12a6, slc5a7, exosc8, sepsecs, atcay, ndufv2,
gars1, ccnf, dnmt1, epm2a, ubtf, stub1, setx, exosc3, tdp2, irf2bpl, xrcc1, fbxo38, tsen54, hspb3, vcp,
eef2, cfap410, atxn3, vldlr, wdr45, pcna, gle1, sncb, tardbp, slc1a3, dnajc6, dao, rars2, fmr1, pmpca,
atp2b3, grm1, toe1, atxn1, ampd2, nek1, matr3, kif5a, tsen15, snx14, fxn, syt14, mapt, jph3, pank2,
vps13a, rubcn, drd4, sacs, exosc9, cacna1g, fbxo7, pde8b, cwf19l1, sorl1, bicd2l, coasy, atp13a2, kif1c, blmh,
tpp1, trpv4, uchl1, aco2, vrk1, slc1a2, park7, xk, sod1, pld3, sptbn2, clp1, c4h19orf12, dab1, atp7a,
kcna1, nhlrc1, mme, vps53, cacnb4, atg5, htt, cacna1a, trpc3, snca, aptx, pik3r5, ccdc88c, ubtf.2, wwox,
pfn1, bicd2, pdyn, lrrk2, eef2.2, sigmar1, rnf170, chmp1a, scyl1, mars2, kcnd3, spg11, vamp1, c1h9orf72, uba1,
tgm6, nop56, tbc1d23, tsen2, dnajc13, sqstm1, tsen34, dctn1, pnkp, syne1, chchd10, plekhg4, slc52a3, tmem240, spg7,
atp8a2, plekhg5, pclo, adh1c, vwa3b, camta1, vps13c, fat2, fig4, nup62, wdr81, ighmbp2, vapb, gba1, atn1,
podxl, jph3.2, bean1
MONDO:0005559 - neurodegenerative disease |
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)