|
DOID:0080015 - physical disorder
Disease Ontology Definition:A disease that has_material_basis_in a genetic abnormality, error with embryonic development, infection or compromised intrauterine environment.
Synonyms: congenital disorder,
Xenbase Genes : foxh1.2, tbx1, hba1, fgg, crx, six3, fga, hras, ar, tll1, hand1, pkd1l1, actc1, zic3, foxe3, [+]
cyp21a2.1, gdf1, tnnt1, zfpm2, gli2, slc4a11, cdh3, igf2, zic2, bmp4, nodal, fgb, pax8, crb1, gdnf,
arx, acvr2b, gata1, prrx1, gli3, gata5, akt1, tfap2b, gata6, ret, hoxd10, tshb, dcn, jag1, slc26a3.2,
mybpc1, slc5a5, nkx2-6, mcph1, gdf3, tbx20, gata4, nphp3, nkx2-5, shh, ptch1, nedd4l, cav1, msx1, brca1,
tubb2b, pten, eed, cntn1, acta1, brip1, trpm1, sptb, gfpt1, alg2, fbn2, mecp2, cited2, dcc, msx2,
alx4, tgif1, erbb3, phox2a, cftr, dnal4, slc26a3.1, neurog3, myo18b, gja1, cyp21a2.2, aspm, tpo, lmna, aipl1,
gmppb, cdon, musk, agpat2, atp6v1b2, cdin1, ube2t, spata7, prkag2, gpi, pomt1, cog6, akr1d1, spint2, ergic1,
pld1, pgm1, snap25, grm6, eml1, nyx, arf1, cog5, hccs, cyp1b1, gucy2c, atp6ap1, dpagt1, lama2, agrn,
neb, foxn1, cog8, bdnf, ezh2, bscl2, gnb3, cers3, col25a1.1, impdh1, zfhx4, g6pd, dnm2, pomgnt1, rpl15,
mmp21, cyp11a1, pde6b, slc5a7, cog2, myo1h, fkrp, slc18a3, rps26, dolk, rho, alg8, rpl26, rps24, ssr4,
rpe65, myh6, rps19, klhl40, rps10, rpl35, stt3b, cog7, fktn, tmem165, gle1, mpi, stt3a, mad2l2, pomgnt2,
hba2, sec23b, iyd, iqcb1, dpm3, stil, atp11c, dpm1, chrna1, rps7, fancl, sumo1, mgat2, chrne, bin1,
ermard, lep, syt2, rps15a, fanci, slx4, lmbr1, scn4a, reln, kcnj13, abcd3, rpl5, chat, gmppa, pomk,
slc35c1, glis3, fancd2, itga7, map3k20, srd5a3, fancc, alg3, epcam, ercc4, slc4a1, nme7, adgrg2, myo5b, cfap53,
mypn, nsd1, cfap52, ntn1, chrnd, nek8, rapsn, slc24a1, kbtbd13, tshr, dcx, mthfd1, myh7, chst3, rtf1,
nmnat1, tsr2, gpr179, tbx22, fancm, cavin1, inpp5k, piga, atp6ap1.2, suz12, alg6, myf6, katnb1, cox7b, col6a3,
col6a1, pmm2, anks3, dpp6, rpl27, star, phox2b, lrat, fanca, rpl11, mtr, slc35a1, lct.2, pcyt1a, mtm1,
rd3, pafah1b1, cfl2, dpm2, gnat1, lca5, mthfr, nde1, rpl18, alg1, cyp17a1, pomt2, b4gat1, nipal4, rpgrip1,
st14, hsd3b7, rxylt1, amacr, cdk5, kif21a, lamb1, rxfp2, slc39a8, b3galnt2, cog1, col12a1, cenpj, tgm1, ryr1,
cacna1f, cdan1, lgi4, gucy2d, cask, pigt, crppa, b4galt1.2, rft1, rad51c, dag1, rpl35a, rps29, rps17, rad51,
trim36, ascl1, fance, foxh1, ift140, cep290, cdk5rap2, tulp1, lmod3, dnah9, mtmr14, dgat1, alg12, ddost, fancf,
usp45, wdpcp, satb2, pip5k1c, mtrr, stx3, tuba1cl.3, ank1, tmem199, acox2, gpr143, klhl41, palb2, b4galt1.1, tmtc3,
tubb3, cyp4f22, ccdc78, cyp7b1, alox12b, mogs, pklr, lct.1, chrna1.2, alg11, specc1l, rps27, chkb, fancg, thra,
col25a1.2, aloxe3, colq, rbfox1, alg9, dok7, frmd7, rfwd3, abca12, arfgef2, map1b, flna, med13l, tpm3, duox2,
knl1, tpm2, tg, cabp4, ubb, lrit3, xrcc2, col6a2, cog4, clcn1, nras, large1, mpdu1, ada2, chrnb1,
col4a1, brca2, edn3, gdf6, selenon, slc35a2, mamld1, col13a1, pnpla1, slc9a3, rho.2, slc26a3.3, tuba1a, cblif, plvap,
epb42, alg13
MONDO:0000839 - obsolete congenital abnormality |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
disease (is_a)