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MeSH keywords -> Related genes, diseases (OMIM)


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01 Kartagener Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
DNAH5 [NCBI] 0.000160229
DNAI1 [NCBI] 0.000129055
DNAH9 [NCBI] 4.56997e-05
DNAH11 [NCBI] 4.46326e-05
FOXJ1 [NCBI] 4.17735e-05
DNASE1 [NCBI] 2.55413e-05
SPAG16 [NCBI] 1.75558e-05
hCG_17324 [NCBI] 1.75558e-05
RP11-529I10.4 [NCBI] 1.75558e-05
DNAH6 [NCBI] 1.75558e-05
DNAH10 [NCBI] 1.75558e-05
DNAL1 [NCBI] 1.75558e-05
DNAH1 [NCBI] 1.51753e-05
KIF3B [NCBI] 1.36935e-05
TXNDC3 [NCBI] 1.36935e-05
FOXI1 [NCBI] 1.26265e-05
KIFAP3 [NCBI] 1.26265e-05
DYNLL1 [NCBI] 1.21652e-05
KIF3A [NCBI] 1.21652e-05
CFTR [NCBI] 1.21185e-05
LEFTY1 [NCBI] 1.13705e-05
NODAL [NCBI] 9.9717e-06
RPGR [NCBI] 7.70523e-06



OMIM


 OMIM Link Information
gain		 01
PCD [NCBI] 0.00648634
kartagener syndrome [NCBI] 0.00414736
immotile cilia syndrome due to defective radial spokes [NCBI] 0.00159179
RA [NCBI] 0.000253937
DNAH5 [NCBI] 0.000159206
DNAH11 [NCBI] 0.000142916
ciliary dyskinesia, primary, 3 [NCBI] 0.000107894
ciliary dyskinesia, primary, 6 [NCBI] 0.000107894
DYNC1I2 [NCBI] 9.57743e-05
DNAH14 [NCBI] 9.57743e-05
DNAH10 [NCBI] 9.57743e-05
DNAH6 [NCBI] 9.57743e-05
TXNDC3 [NCBI] 9.57743e-05
DYNC2H1 [NCBI] 8.19941e-05
DYNLL2 [NCBI] 8.19941e-05
DYNLRB2 [NCBI] 8.19941e-05
DNAH2 [NCBI] 8.19941e-05
DYNC1H1 [NCBI] 8.19941e-05
DNAI1 [NCBI] 8.19941e-05
DNAH7 [NCBI] 8.19941e-05
DNAH12 [NCBI] 8.19941e-05
DNAH8 [NCBI] 8.19941e-05
DYNLL1 [NCBI] 7.67933e-05
DNAH9 [NCBI] 7.67933e-05
FOXJ1 [NCBI] 7.34161e-05
ciliary discoordination due to random ciliary orientation [NCBI] 7.14934e-05
retinitis pigmentosa, x-linked, with recurrent respiratory infections [NCBI] 6.74182e-05
situs inversus viscerum [NCBI] 5.91783e-05
CFTR [NCBI] 4.78583e-05
RPGR [NCBI] 4.59419e-05
usher syndrome, type i [NCBI] 3.45473e-05
RP [NCBI] 2.56541e-05
BBS [NCBI] 1.57335e-05
CF [NCBI] 1.26856e-05



Database Center for Life Science