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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, cst8, LOC101731116
| MONDO:0005283 - tela choroidea |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s):
eye disease (is_a)
