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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00001 |
B-cell acute lymphoblastic leukemia B-cell acute lymphocytic leukemia |
... translocation that results in expression of the TCF3 (E2A) fusion partner, (also known as TCF3) TFPT-PBX1 fusion (E2A-PBX); the t(9;22) (q34;q11.2) "Philadelphia" chromosome resulting in expression of the ... | Cancer |
BCR-ABL (translocation) [HSA:25] [KO:K06619] MLL-AF4 (translocation) [HSA:4297 4299] [KO:K09186 K15184] E2A-PBX1 (translocation) [HSA:6929 5087] [KO:K09063 K09355] TEL-AML1 (translocation) [HSA:861] [KO:K08367] c-MYC (rearrangement) [HSA:4609] [KO:K04377] CRLF2 (rearrangement) [HSA:64109] [KO:K05078] PAX5 (rearrangement) [HSA:5079] [KO:K09383] |
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| H01867 | Congenital anomalies of kidney and urinary tract | Congenital anomalies of the kidney and urinary tract (CAKUT) include a wide range of structural malformations resulting from defects in the morphogenesis of the kidney and of the urinary tract. CAKUT represent ... | Congenital malformation |
(CAKUT1) DSTYK [HSA:25778] [KO:K16288] (CAKUT2) TBX18 [HSA:9096] [KO:K10183] (CAKUT3) NRIP1 [HSA:8204] [KO:K17965] (CAKUTHED) PBX1 [HSA:5087] [KO:K09355] |
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