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DOID:0050889 - non-syndromic intellectual disability
Disease Ontology Definition:An intellectual disability that is characterized by the absence of associated medical and behavioral signs and symptoms.
Synonyms:
Xenbase Genes : tnik, sox4, rps6ka3, tbl1xr1, smarce1, il1rapl1, sox11, arx, smarca4, ezr, hivep2, mef2c, ctnnb1, syngap1, slc9a7, [+]
csnk2b, rac1, rab11a, smarcc2, cnksr2, arid1a, tbcd, rab39b, smarcb1, grin1, kptn, mecp2, kmt5b, adnp, dmd.2,
tusc3, cux1, dync1h1, kdm5b, ctcf, camk2a, camk2b, epb41l1, lingo1, agtr2, kirrel3, trio, st3gal3, tspan7, syp,
stxbp1, dpf2, pgap3, dcps, zdhhc15, grin2b, arhgef6, clcn4, pigc, ppp3ca, fbxo31, ndst1, slc45a1, taok1, znf711,
lins1, aimp1, wars2, naa15, kif1a, zmynd11, pak3, nsun2, slc6a17, cacng2, pigv, ogt, taf2, sars1, pura,
crbn, eef1a2, pigw, dlg3, mboat7, nus1, zc3h14, cdh15, cltc, prss12, set, hsd17b10, dock8, auts2, myt1l,
ank3, kcnq5, ppp2r1a, rusc2, upf3b, ferry3, apc2, chd4, magt1, dpp6, lman2l, tti2, hnmt, gemin4, cert1,
klhl15, tecr, zbtb18, med23, impa1, stag1, ufc1, arid1b, usp9x, tcf4, b3galnt2, mid2, herc2, clip1, champ1,
dyrk1a, deaf1, znf238.2, elp2, cradd.2, brwd3, dyrk1a.2, pigy, taf13, ftsj1, cc2d1a, steep1, rsrc1, dmd, dmd,
pgap1, med25, ahdc1, setd5, trappc9, cradd.1, man1b1, edc3, setbp1, gdi1, mbd5, washc4, kif4a, znf674, pigo,
fmn2, acsl4, gatad2b, mettl23, ash1l, iqsec2, trpm3, znf81, nexmif, grik2, frmpd4, bptf, arid2, trip12, kat6a,
gnb1, hcfc1, frrs1l, pogz, adat3, pacs1, pgap2, cic, brsk2, alg13
MONDO:0000509 - non-syndromic intellectual disability |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
intellectual disability (is_a)