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DOID:0080012 - X-linked recessive disease
Disease Ontology Definition:A X-linked monogenic disease that has_material_basis_in recessive inheritance.
Synonyms:
Xenbase Genes
ndp, dmd.2, spag1, foxj1, dnah5, dnai2, odad3, foxj1.2, dnah1, dnaaf19, zc4h2, f9, tspan7, cfap300, dnaaf11,
pgk1, xiap, nyx, dnah11, aff2, taf1, atp6ap1, abcd1, mbtps2, sms, pex10, opn1lw, dnaaf4, gas2l2, wipf1,
zmynd10, pak3, las1l, fhl1, atp6ap2, gas8, ssr4, pex26, gpc4, atp11c, dlg3, atp2b3, cybb, ikbkg, ccdc22,
ccno, hydin, abcb7, thoc2, slc16a2, gpc3, rpgr, odad2, dnal1, pex1, med12, eif2s3, ccdc40, ccdc39, rsph3,
ocrl, pof1b, ammecr1, dnaaf6, phf8, tsr2, phka2, dnajb13, piga, atp6ap1.2, myf6, phf6, cenpf, ccdc65, klhl15,
sat1, bgn, msn, nsdhl, ap1s2, prps1, plp1, pex5, tafazzin, atp7a, usp9x, ofd1, mid2, sts, pex13,
cacna1f, hprt1, cask, aifm1, f8, kdm5c, avpr2c, vma21, maoa, dnah9, brwd3, was, dkc1, ftsj1, dmd.3,
dmd, spef2, rs1, hdac8, uba1, arsl, lage3, dnaaf2, dnaaf5, gdi1, cfap298, l1cam, kif4a, znf674, rsph9,
cfp, rsph1, clcn5, odad4, drc1, phka1, stk36, tex11, flna, lrrc56, arsl, frmpd4, sh2d1a, hcfc1, dnaaf3,
btk, fgd1, ebp, pqbp1, dnai1, foxp3, eda, cfap221, mcidas, spn, dnaaf1, fancb
| MONDO:0020605 - X-linked recessive disease |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s):
X-linked monogenic disease (is_a)
