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Entry Name Description Category Pathway Gene
H00564 Primary ciliary dyskinesia Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder with recurrent oto-sinopulmonary infections, bronchiectasis, and infertility owing to impaired motile ciliary function. Alterations in ... Respiratory disease (CILD1) DNAI1 [HSA:27019] [KO:K10409]
(CILD2) DNAAF3 [HSA:352909] [KO:K19752]
(CILD3) DNAH5 [HSA:1767] [KO:K10408]
(CILD5) HYDIN [HSA:54768] [KO:K17570]
(CILD6) TXNDC3 [HSA:51314] [KO:K19868]
(CILD7) DNAH11 [HSA:8701] [KO:K10408]
(CILD9) DNAI2 [HSA:64446] [KO:K11143]
(CILD10) KTU [HSA:55172] [KO:K19751]
(CILD11) RSPH4A [HSA:345895] [KO:K19756]
(CILD12) RSPH9 [HSA:221421] [KO:K19757]
(CILD13) LRRC50 [HSA:123872] [KO:K19750]
(CILD14) CCDC39 [HSA:339829]
(CILD15) CCDC40 [HSA:55036]
(CILD16) DNAL1 [HSA:83544] [KO:K10411]
(CILD17) CCDC103 [HSA:388389]
(CILD18) HEATR2 [HSA:54919] [KO:K19759]
(CILD19) LRRC6 [HSA:23639] [KO:K19753]
(CILD20) CCDC114 [HSA:93233]
(CILD21) DRC1 [HSA:92749] [KO:K19754]
(CILD22) ZMYND10 [HSA:51364]
(CILD23) ARMC4 [HSA:55130]
(CILD24) RSPH1 [HSA:89765] [KO:K19755]
(CILD25) DYX1C1 [HSA:161582] [KO:K19758]
(CILD26) C21ORF59 [HSA:56683]
(CILD27) CCDC65 [HSA:85478]
(CILD28) SPAG1 [HSA:6674] [KO:K19870]
(CILD29) CCNO [HSA:10309] [KO:K10861]
(CILD30) CCDC151 [HSA:115948]
(CILD32) RSPH3 [HSA:83861]
(CILD33) GAS8 [HSA:2622] [KO:K19942]
(CILD34) DNAJB13 [HSA:374407] [KO:K09519]
(CILD35) TTC25 [HSA:83538]
(CILD36) PIH1D3 [HSA:139212]
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