| 
 | 
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
 :
		
					
			
			bmp15,
			
			
		
		
			
						
		
					
			
			ar,
			
			
		
		
			
						
		
					
			
			bcap31,
			
			
		
		
			
						
		
					
			
			pou3f4,
			
			
		
		
			
						
		
					
			
			zic3,
			
			
		
		
			
						
		
					
			
			rps6ka3,
			
			
		
		
			
						
		
					
			
			gjb1,
			
			
		
		
			
						
		
					
			
			avpr2,
			
			
		
		
			
						
		
					
			
			il2rg,
			
			
		
		
			
						
		
					
			
			il1rapl1,
			
			
		
		
			
						
		
					
			
			fgf16,
			
			
		
		
			
						
		
					
			
			arx,
			
			
		
		
			
						
		
					
			
			gata1,
			
			
		
		
			
						
		
					
			
			sox3,
			
			
		
		
			
						
		
					
			
			alas2,
			
			
		
		
							[+]
:
		
					
			
			bmp15,
			
			
		
		
			
						
		
					
			
			ar,
			
			
		
		
			
						
		
					
			
			bcap31,
			
			
		
		
			
						
		
					
			
			pou3f4,
			
			
		
		
			
						
		
					
			
			zic3,
			
			
		
		
			
						
		
					
			
			rps6ka3,
			
			
		
		
			
						
		
					
			
			gjb1,
			
			
		
		
			
						
		
					
			
			avpr2,
			
			
		
		
			
						
		
					
			
			il2rg,
			
			
		
		
			
						
		
					
			
			il1rapl1,
			
			
		
		
			
						
		
					
			
			fgf16,
			
			
		
		
			
						
		
					
			
			arx,
			
			
		
		
			
						
		
					
			
			gata1,
			
			
		
		
			
						
		
					
			
			sox3,
			
			
		
		
			
						
		
					
			
			alas2,
			
			
		
		
							[+]
							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)
				
				
			
		
		