Search Result |
Top |
Entry | Name | Description | Category | Pathway | Gene |
---|---|---|---|---|---|
H00751 |
Asphyxiating thoracic dystrophy Jeune syndrome |
Asphyxiating thoracic dystrophy (ATD), also known as Jeune syndrome, is a rare osteochondrodysplasia with characteristic skeletal abnormalities as well as the involvement of kidneys, liver, pancreas and ... | Congenital malformation |
(ATD2) IFT80 [HSA:57560] [KO:K19678] (ATD3) DYNC2H1 [HSA:79659] [KO:K10414] (ATD4) TTC21B [HSA:79809] [KO:K19673] (ATD5) WDR19 [HSA:57728] [KO:K19671] |
|
H02157 | Short-rib thoracic dysplasia | Short-rib thoracic dysplasia (SRTD) is a group of autosomal recessive skeletal ciliopathies. The ciliary machinery has been implicated in more than a dozen disorders, now called ciliopathies. Primary cilia ... | Congenital malformation |
(SRTD2) IFT80 [HSA:57560] [KO:K19678] (SRTD3) DYNC2H1 [HSA:79659] [KO:K10414] (SRTD4) TTC21B [HSA:79809] [KO:K19673] (SRTD5) WDR19 [HSA:57728] [KO:K19671] (SRTD6) NEK1 [HSA:4750] [KO:K08857] (SRTD7) WDR35 [HSA:57539] [KO:K19674] (SRTD8) DYNC2I1 [HSA:55112] [KO:K22869] (SRTD9) IFT140 [HSA:9742] [KO:K19672] (SRTD10) IFT172 [HSA:26160] [KO:K19676] (SRTD11) DYNC2I2 [HSA:89891] [KO:K22868] (SRTD13) CEP120 [HSA:153241] [KO:K16459] (SRTD14) JBTS23 [HSA:9786] [KO:K22865] (SRTD15) DYNC2LI1 [HSA:51626] [KO:K10417] (SRTD16) IFT52 [HSA:51098] [KO:K19681] (SRTD17) DYNLT2B [HSA:255758] [KO:K22866] (SRTD18) IFT43 [HSA:112752] [KO:K19675] (SRTD19) IFT81 [HSA:28981] [KO:K19677] (SRTD20) INTU [HSA:27152] [KO:K22862] (SRTD21) JBTS38 [HSA:9851] [KO:K21765] |
[ KEGG | DISEASE | DRUG | MEDICUS ] |