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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

foxe3, cyp21a2, gdf1, tnnt1, zfpm2, gli2, slc4a11, csf3r, 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, 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, sag, hccs, cyp1b1, gucy2c, arhgef38,
atp6ap1, dpagt1, lama2, agrn, neb, foxn1, cog8, bdnf, ezh2, bscl2, gnb3, cers3, col25a1, impdh1, zfhx4,
g6pd, dnm2, pomgnt1, rpl15, mmp21, gfi1, pign, cyp11a1, pde6b, slc5a7, vps45, cog2, myo1h, fkrp, slc18a3,
rps26, dolk, rho, alg8, rps24, ssr4, rpe65, myh6, rps19, klhl40, rps10, rpl35, stt3b, cog7, fktn,
tmem165, gle1, mpi, stt3a, mad2l2, pomgnt2, hba2, pmm2, sec23b, iyd, iqcb1, dpm3, stil, atp11c, gss,
dpm1, chrna1, rps7, g6pc3, 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, g6pc3.2, nme7, adgrg2, myo5b, cfap53, mypn, nsd1, cfap52, ntn1, chrnd,
nek8, rapsn, slc24a1, kbtbd13, tshr, dcx, mthfd1, myh7l, chst3, rtf1, nmnat1, tsr2, gpr179, tbx22, fancm,
cavin1, inpp5k, piga, atp6ap1.2, suz12, alg6, myf6, katnb1, cox7b, col6a3, col6a1, anks3, dpp6, rpl27, star,
phox2b, lrat, fanca, rpl11, mtr, slc35a1, lct.2, pcyt1a, ric1, mtm1, rd3, gclc, 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, grk1, cpap, plcd1, 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, was, dgat1, alg12, ddost, ccdc115, fancf,
usp45, wdpcp, satb2, pip5k1c, mtrr, stx3, tuba1cl.3, ank1, tmem199, acox2, gpr143, klhl41, palb2, b4galt1, tmtc3,
tubb3, cyp4f22, ccdc78, cyp7b1, alox12b, hax1, mogs, pklr, lct, chrna1.2, alg11, specc1l, jagn1, rps27, chkb,
fancg, thra, col25a1.2, cobll1, 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, col7a1, plvap, epb42, alg13, mpl
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)