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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

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: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
disease (is_a)