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DOID:5679 - retinal disease
Disease Ontology Definition:An eye disease that is located_in the retina.
Synonyms:
Xenbase Genes

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,
nek2l, 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, nek2, LOC101731116
MONDO:0005283 - tela choroidea |
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)