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DOID:5679 - retinal disease
Disease Ontology Definition:An eye disease that is located_in the retina.
Synonyms:
Xenbase Genes : c2, fzd4, rab28, crx, cdhr1, cfb, ctnna1, crb1, pax6, lrp5, otx2, nr2e3, ift88, c3, pde6c, [+]
ctnnb1, htra1, prpf31, mak, tlr3, trpm1, mertk, prpf4, rax2, fscn2, ndp, apoe, prom1, mapkapk3, aipl1,
bbs2, kcnv2, arl6, spata7, arl2bp, rp9, poc1b, pde6g, capn5, cnga3, grm6, nyx, sag, cnga1, elovl4,
unc119, opn1lw, chm, arl3, gnb3, ush2a, impdh1, agbl5, pomgnt1, rp1l1, znf408, pde6b, rp2, tub, rom1,
nek2, prpf8, rho, c9, rpe65, cfap410, klhl7, reep6, iqcb1, rlbp1, adam9, cyp4v2.2, cngb1, cfh, snrnp200,
rpgr, ahr, kcnj13, pitpnm3, atf6, impg2, ca4, hgsnat, prph2, pde6a, dhx38, best1, arhgef18, cacna2d4, slc24a1,
opn1sw, nmnat1, gpr179, topors, prpf3, prpf6, ttc8, lrat, abca4, pcyt1a, dhdds, rd3, gnat1, lca5, rpgrip1,
rbp3, slc7a14, ofd1, rgr, rgs9bp, tspan12, c1qtnf5, efemp1, grk1, rims1, cacna1f, gucy2d, znf513, plekha1, rb1,
ift140, ift172, cep290, tulp1, guca1al, slc38a8, tbc1d32, usp45, fam161a, idh3b, arl3l2, rs1, cst3, ahi1, ttll5,
kiz, ift43, sema4a, rgs9bpl, ca4.2, cfi, scaper, rgs9, pde6h, rp1, cerkl, cngb3, clrn1, cabp4, lrit3,
KIAA1549, hmcn1, gnat2, gdf6, nrl, cfap418, tlr4, pcare, rho.2, guca1a, guca1b, LOC100328980, LOC101731116
MONDO:0005283 - retinal disorder |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
eye disease (is_a)