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DOID:0050735 - X-linked monogenic disease
Disease Ontology Definition:A monogenic disease that has_material_basis_in mutations in genes on the X chromosome.
Synonyms:
Xenbase Genes
slc9a7, nr0b1, anos1, cd40lg, smpx, cnksr2, igbp1, rlim, rab39b, mid1, mecp2, amelx, ndp, dmd.2, spag1,
foxj1, cftr, dnah5, dnai2, odad3, foxj1.2, dnah1, porcn, dnaaf19, agtr2, zc4h2, f9, tspan7, cfap300, syp,
dnaaf11, pgk1, xiap, zdhhc15, arhgef6, nyx, clcn4, dnah11, cdkl5, hccs, aff2, taf1, atp6ap1, abcd1, mbtps2,
sms, pex10, opn1lw, gjb2, znf711, huwe1, dnaaf4, gas2l2, wipf1, zmynd10, rp2, pak3, las1l, lamp2, cul4b,
fhl1, atp6ap2, pdk3, gas8, ogt, naa10, ssr4, ube2a, pex26, wdr45, gpc4, atp11c, fmr1, dlg3, atp2b3,
cybb, ikbkg, ccdc22, ccno, hydin, abcb7, thoc2, atrx, slc16a2, gpc3, rpgr, odad2, dnal1, pex1, med12,
eif2s3, ccdc40, hsd17b10, adgrg2, ccdc39, rsph3, ocrl, pof1b, ammecr1, dnaaf6, phf8, tsr2, upf3b, phka2, tbx22,
dnajb13, piga, atp6ap1.2, myf6, cox7b, magt1, phf6, pola1, hmgb3, cenpf, nono, ccdc65, klhl15, sat1, bgn,
msn, nsdhl, xk, ap1s2, prps1, plp1, pex5, tafazzin, gria3, atp7a, usp9x, bcor, ofd1, efnb1, phex,
mid2, sts, pex13, cacna1f, hprt1, cask, zdhhc9, aifm1, f8, kdm5c, pcdh19, avpr2c, vma21, rbmx, maoa,
dnah9, brwd3, was, dkc1, ftsj1, steep1, dmd.3, dmd, spef2, rs1, hdac8, nhs, hdac6, uba1, arsl,
lage3, dnaaf2, dnaaf5, gdi1, cfap298, l1cam, kif4a, znf674, rsph9, cfp, rsph1, shroom4, clcn5, odad4, acsl4,
drc1, phka1, stk36, col4a6, iqsec2, znf81, col4a5, nexmif, tex11, flna, lrrc56, slc9a6, arsl, frmpd4, sh2d1a,
hcfc1, rnf113a, dnaaf3, diaph2, syn1, btk, fgd1, ebp, pqbp1, dnai1, slc35a2, foxp3, eda, cfap221, mcidas,
spn, dnaaf1, alg13, fancb
| MONDO:0000425 - X-linked disease |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s):
monogenic disease (is_a)
