67 results in total
All the pertinent items are shown as follows. Please click which you’d like to display for more information and then move forward to the Demo function.
ID | Organism | Tissue | Karyotype | Diseases |
---|---|---|---|---|
iBAD_0000001 | Homo sapiens | Embryo | monosomy 1 | - |
iBAD_0000002 | Homo sapiens | Embryo | monosomy 2 | - |
iBAD_0000003 | Homo sapiens | Embryo | monosomy 3 | - |
iBAD_0000004 | Homo sapiens | Embryo | monosomy 4 | - |
iBAD_0000005 | Homo sapiens | Embryo | monosomy 5 | Criduchat syndrome |
iBAD_0000006 | Homo sapiens | Embryo | monosomy 6 | - |
iBAD_0000007 | Homo sapiens | Embryo | monosomy 7 | Williams syndrome |
iBAD_0000008 | Homo sapiens | Embryo | monosomy 8 | - |
iBAD_0000009 | Homo sapiens | Embryo | monosomy 9 | - |
iBAD_0000010 | Homo sapiens | Embryo | monosomy 10 | - |
iBAD_0000011 | Homo sapiens | Embryo | monosomy 11 | - |
iBAD_0000012 | Homo sapiens | Embryo | monosomy 12 | - |
iBAD_0000013 | Homo sapiens | Embryo | monosomy 13 | - |
iBAD_0000014 | Homo sapiens | Embryo | monosomy 14 | - |
iBAD_0000015 | Homo sapiens | Embryo | monosomy 15 | Prader–Willi syndrome; Angelman syndrome |
iBAD_0000016 | Homo sapiens | Embryo | monosomy 16 | - |
iBAD_0000017 | Homo sapiens | Embryo | monosomy 17 | - |
iBAD_0000018 | Homo sapiens | Embryo | monosomy 18 | - |
iBAD_0000019 | Homo sapiens | Embryo | monosomy 19 | - |
iBAD_0000020 | Homo sapiens | Embryo | monosomy 20 | - |
iBAD_0000021 | Homo sapiens | Embryo | monosomy 21 | - |
iBAD_0000022 | Homo sapiens | Embryo | monosomy 22 | - |
iBAD_0000023 | Homo sapiens | Embryo | monosomy XO | Turner syndrome |
iBAD_0000024 | Homo sapiens | Embryo | Trisomy 1 | - |
iBAD_0000025 | Homo sapiens | Embryo | Trisomy 2 | - |
iBAD_0000026 | Homo sapiens | Embryo | Trisomy 3 | - |
iBAD_0000027 | Homo sapiens | Embryo | Trisomy 4 | - |
iBAD_0000028 | Homo sapiens | Embryo | Trisomy 5 | - |
iBAD_0000029 | Homo sapiens | Embryo | Trisomy 6 | - |
iBAD_0000030 | Homo sapiens | Embryo | Trisomy 7 | - |
iBAD_0000031 | Homo sapiens | Embryo | Trisomy 8 | Warkany syndrome 2 |
iBAD_0000032 | Homo sapiens | Embryo | Trisomy 9 | - |
iBAD_0000033 | Homo sapiens | Embryo | Trisomy 10 | - |
iBAD_0000034 | Homo sapiens | Embryo | Trisomy 11 | - |
iBAD_0000035 | Homo sapiens | Embryo | Trisomy 12 | - |
iBAD_0000036 | Homo sapiens | Embryo | Trisomy 13 | Patau syndrome |
iBAD_0000037 | Homo sapiens | Embryo | Trisomy 14 | - |
iBAD_0000038 | Homo sapiens | Embryo | Trisomy 15 | - |
iBAD_0000039 | Homo sapiens | Embryo | Trisomy 16 | - |
iBAD_0000040 | Homo sapiens | Embryo | Trisomy 17 | - |
iBAD_0000041 | Homo sapiens | Embryo | Trisomy 18 | Trisomy 18 syndrome |
iBAD_0000042 | Homo sapiens | Embryo | Trisomy 19 | - |
iBAD_0000043 | Homo sapiens | Embryo | Trisomy 20 | - |
iBAD_0000044 | Homo sapiens | Embryo | Trisomy 21 | Down syndrome |
iBAD_0000045 | Homo sapiens | Embryo | Trisomy 22 | - |
iBAD_0000046 | Homo sapiens | Embryo | Trisomy XXX | Triple X syndrome |
iBAD_0000047 | Homo sapiens | Embryo | Trisomy XXY | Klinefelter syndrome |
iBAD_0000048 | Homo sapiens | IPSC | Trisomy 21 | Down syndrome |
iBAD_0000049 | Homo sapiens | IPSC | Trisomy 21 | Down syndrome |
iBAD_0000056 | Homo sapiens | Connective | Trisomy 21 | Down syndrome |
iBAD_0000057 | Homo sapiens | IPSC | Trisomy 21 | Down syndrome |
iBAD_0000058 | Homo sapiens | Connective | Trisomy 21 | Down syndrome |
iBAD_0000060 | Homo sapiens | IPSC | Trisomy 21 | Down syndrome |
iBAD_0000061 | Homo sapiens | Maternal uterine | Trisomy 21 | Down syndrome |
iBAD_0000062 | Homo sapiens | Blood | Trisomy 21 | Down syndrome |
iBAD_0000063 | Homo sapiens | Connective | Trisomy 21 | Down syndrome |
iBAD_0000064 | Homo sapiens | Lymphoid | Trisomy 21 | Down syndrome |
iBAD_0000065 | Homo sapiens | Connective | Trisomy 21 | Down syndrome |
iBAD_0000067 | Homo sapiens | Lymphoid | Trisomy 21 | Down syndrome |
iBAD_0000068 | Homo sapiens | Blood | Trisomy 21 | Down syndrome |
iBAD_0000074 | Homo sapiens | IPSC | Trisomy 8, Trisomy 13, Trisomy 22, monosomy X | Warkany syndrome 2; Patau syndrome |
iBAD_0000076 | Homo sapiens | IPSC | monosomy X | Turner syndrome |
iBAD_0000077 | Homo sapiens | Gonadal | Trisomy XXY | Klinefelter syndrome |
iBAD_0000078 | Homo sapiens | Gonadal | Trisomy XXY | Klinefelter syndrome |
iBAD_0000079 | Homo sapiens | Gonadal | Trisomy XXY | Klinefelter syndrome |
iBAD_0000080 | Homo sapiens | Gonadal | Trisomy XXY | Klinefelter syndrome |
iBAD_0000081 | Homo sapiens | Gonadal | Trisomy XXY | Klinefelter syndrome |