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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, 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
MONDO:0000425 - X-linked disease |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
monogenic disease (is_a)