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DOID:1059 - intellectual disability
Disease Ontology Definition:A specific developmental disorder that involves significant limitations both in mental functioning and in adaptive behavior such as communicating, taking care of him or herself, and social skills.
Synonyms: mental retardation, MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
Xenbase Genes

csnk2b, rac1, rab11a, smarcc2, cnksr2, igbp1, rlim, arid1a, tbcd, rab39b, smarcb1, grin1, kptn, mecp2, kmt5b,
adnp, dmd.2, tusc3, cux1, dync1h1, kdm5b, ctcf, camk2a, camk2b, epb41l1, lingo1, agtr2, kirrel3, trio, st3gal3,
zc4h2, tspan7, syp, stxbp1, dpf2, pgap3, dcps, zdhhc15, grin2b, arhgef6, clcn4, pigc, aff2, ppp3ca, nrxn1,
sms, fbxo31, ndst1, slc45a1, taok1, znf711, lins1, huwe1, aimp1, wars2, dnmt3a, naa15, kif1a, zmynd11, foxp1,
pak3, las1l, nsun2, cul4b, atp6ap2, slc6a17, cacng2, pigv, ogt, taf2, sars1, ube2a, pura, crbn, eef1a2,
pigw, dlg3, mboat7, thoc2, nus1, zc3h14, cdh15, cltc, prss12, med12, eif2s3, set, hsd17b10, dock8, auts2,
myt1l, ank3, kcnq5, ppp2r1a, phf8, rusc2, upf3b, ferry3, apc2, chd4, magt1, dpp6, lman2l, phf6, tti2,
hnmt, gemin4, cert1, nono, klhl15, tecr, zbtb18, med23, impa1, stag1, ap1s2, prps1, ophn1, ufc1, arid1b,
gria3, ube3b, usp9x, tcf4, b3galnt2, mid2, herc2, clip1, cask, champ1, zdhhc9, dyrk1a, kdm5c, deaf1, znf238.2,
rbmx, elp2, cradd.2, brwd3, dyrk1a.2, pigy, taf13, ftsj1, cc2d1a, steep1, rsrc1, dmd.3, dmd, pgap1, med25,
ahdc1, setd5, trappc9, cradd, hdac8, man1b1, edc3, setbp1, gdi1, arhgef2, mbd5, washc4, kif4a, znf674, pigo,
shroom4, fmn2, acsl4, gatad2b, mettl23, ash1l, iqsec2, trpm3, znf81, nexmif, slc9a6, grik2, frmpd4, bptf, arid2,
trip12, kat6a, gnb1, hcfc1, frrs1l, pogz, adat3, pacs1, pgap2, pqbp1, cic, brsk2, alg13
MONDO:0001071 - superficial cervical artery |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
specific developmental disorder (is_a)