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DOID:5614 - eye disease
Disease Ontology Definition:An eye and adnexa disease that is located_in the eye.
Synonyms:
Xenbase Genes : c2, fzd4, rab28, vax1, crx, cdhr1, foxc1, cfb, ctnna1, foxe3, rarb, mfrp, slc4a11, timp3, pitx2, [+]
bmp4, six6, crb1, pax6, sox2, mip, zeb1, mitf, wt1, lrp5, otx2, dcn, nr2e3, grhl2, pitx3,
ift88, c3, pde6c, ctnnb1, gdf3, htra1, shh, prpf31, gsn, gcnt2.2, mak, tlr3, tubb2b, trpm1, rax,
vim, mertk, gja8, prpf4, gja3, sall2, rax2, lmx1b, smarca5, fscn2, bap1, ndp, vsx1, apoe, vsx2,
prom1, phox2a, ovol2, prdm5, mapkapk3, lmx1b.2, vim.2, aipl1, bbs2, pxdn, kcnv2, arl6, sco2, chmp4b, spata7,
arl2bp, optn, gna11, tdrd7, rp9, poc1b, pde6g, lrpap1, capn5, cnga3, grm6, nyx, agbl1, sag, chn1,
cnga1, hccs, cyp1b1, slc39a5, elovl4, fbn1, unc119, opn1lw, cryba1, chm, arl3, gnb3, ush2a, col25a1.1, impdh1,
zfhx4, agbl5, pomgnt1, rp1l1, znf408, chst6, pde6b, col8a2, rp2, bfsp2, tub, rom1, nek2, ubiad1, cryba2,
naa10, prpf8, rho, c9, rpe65, cfap410, cryab, klhl7, unc45b, wdr36, snx3, gnaq, reep6, iqcb1, rlbp1,
adam9, cyp4v2.2, lim2, wfs1, znf644, agk, cngb1, bfsp1, cfh, snrnp200, rpgr, ahr, kcnj13, mab21l2, pitpnm3,
atf6, atf4, impg2, ca4.1, hgsnat, cpamd8, prph2, adamtsl4, tyr, pde6a, atoh7, pikfyve, dhx38, best1, arhgef18,
cacna2d4, slc24a1, elp4, aldh1a3, opn1sw, nmnat1, gpr179, topors, prpf3, prpf6, cox7b, crybb1, cryba4, ttc8, lrat,
abca4, pcyt1a, hmgb3, stra6, loxl1, dhdds, rd3, gnat1, lca5, oat.2, rpgrip1, rbp3, slc7a14, kif21a, bcor,
ofd1, rgr, rgs9bp, tcf4, rdh5, tspan12, c1qtnf5, efemp1, grk1, kera, rims1, slc16a12, ntf4, cacna1f, gucy2d,
znf513, plekha1, rb1, krt12.5, ift140, ift172, cep290, tulp1, tgfbi, guca1al, epha2, slc38a8, lss, tbc1d32, crybb3,
usp45, fam161a, idh3b, arl3l2, gpr143, rs1, tmem98, crybb2, nhs, cst3, ahi1, tubb3, ttll5, kiz, tead1,
ift43, sema4a, primpol, rgs9bpl, cryaa, ca4.2, cfi, scaper, rgs9, krt12.1, col25a1.2, oat, pde6h, rp1, cerkl,
cngb3, frmd7, clrn1, prss56, maf, cabp4, lrit3, mafb, KIAA1549, myoc, hmcn1, gnat2, gdf6, nrl, znf469,
cfap418, col17a1, krt12.6, tlr4, krt12.2, krt12.4, pcare, rho.2, krt12.3, guca1a, cryba1.2, hsf4, guca1b
MONDO:0005328 - eye disorder |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
sensory system disease (is_a)