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DOID:0060038 - specific developmental disorder
Disease Ontology Definition:A developmental disorder of mental health that categorizes specific learning disabilities and developmental disorders affecting coordination.
Synonyms:
Xenbase Genes

slc9a7, 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, bdnf, taok1, znf711, lins1, huwe1, aimp1, wars2, dnmt3a, naa15, kif1a,
zmynd11, foxp1, pak3, las1l, nsun2, cul4b, atp6ap2, slc6a17, tm4sf20, cacng2, pigv, ogt, taf2, sars1, ube2a,
pura, crbn, eef1a2, pigw, dlg3, mboat7, hdc, thoc2, nus1, slc6a3, zc3h14, cdh15, cltc, prss12, med12,
eif2s3, set, hsd17b10, dock8, auts2, myt1l, ap4e1, ank3, kcnq5, drd4, ppp2r1a, drd5, phf8, rusc2, upf3b,
ferry3, apc2, chd4, magt1, slitrk1, 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, dcdc2, 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, KIAA0319, adat3, pacs1, pgap2, pqbp1, cic, brsk2, alg13
MONDO:0000592 - decreased thickness |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee