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DOID:863 - nervous system disease
Disease Ontology Definition:A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system.
Synonyms:
Echinobase Genes

sgcb, pou4f3, spart, LOC585120, inf2, brca2, agk, rubcn, slc2a1, mars2, tbc1d24, col4a1, myo7a, sox2, capn5,
rb1, pdcd10, aptx, LOC586864, cspp1, otof, washc5, ccm2, LOC587274, stub1, LOC582974, ap5z1, aco2, prpf31, nt5c2,
prom1, dctn1, idh3b, sufu, nmnat1, snrnp200, ubiad1, slc7a14, park7, opa1, gch1, pde6d, pex5, epha2, LOC578254,
cep290, tmem138, tead1, ascl1, aspm, elovl4, pax6, sepsecs, clp1, atxn10, tmem98, kars1, hspd1, LOC373238, pnkd,
vps53, prpf8, smarcb1, trappc11, lztr1, rp2, synj1, lca5, rars2, yars1, chmp2b, rpgr, fig4, dhdds, arl13b,
sod1, arl6, dmd, stil, sptlc1, eif2b2, c9orf72, cplane1, pomgnt1, eif2b3, exosc3, kif2a, wdr45, slc4a11, hccs,
ptch1, sptan1, stxbp2, c3, pomt1, lrsam1, prpf4, whrn, vsx2, tdp1, l2hgdh, opa3, ddhd1, dhtkd1, wdr81,
gphn, spata7, nkx2-1, otx2, dync1h1, pnpt1, pomt2, selenon, six6, six1, psen1, tbp, tecpr2, vrk1, ermard,
b3galnt2, nphp1, ap4m1, b4gat1, spast, opn1lw, LOC581885, ap4e1, crppa, cep152, mtpap, gmppb, cep41, lrrk2, rab7a,
msrb3, adam10, LOC582206, rxylt1, dag1, itpr1, ap4b1, colq, als2, a2m, tsen2, prpf6, efhc1, ctnnb1, gosr2,
nr4a2, LOC594147, zfhx4, arl2bp, tmem67, rpgrip1l, spg7, LOC594592, ca8, foxc1, ano10, tmem231, gnao1, pnkp, LOC575087,
aars1, gnal, afg3l2, c8orf37, pomgnt2, vps35, spg21, nr2e3, aldh7a1, eif2b5, eef2, gba2, rgs9bp, elp1, mt-nd1,
mt-nd2, mt-co1, ND4L, mt-atp6, mt-co3, mt-nd4, mt-nd5, ND6, mt-cyb
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
disease of anatomical entity (is_a)