All terms in CLO
| Label | Id | Description |
|---|---|---|
| IMG-766 cell | CLO_0006863 | |
| IMG-765 cell | CLO_0006862 | |
| Hs 895.T cell | CLO_0004200 | [disease: melanoma (skin primary)] |
| IMG-763 cell | CLO_0006861 | |
| GM04519 cell | CLO_0018846 | [ TUBEROUS SCLEROSIS; TS TSC2 GENE; TSC2] |
| GM16107 cell | CLO_0018847 | [ CEROID LIPOFUSCINOSIS, NEURONAL 1, INFANTILE; CLN1 PALMITOYL-PROTEIN THIOESTERASE 1; PPT1] |
| GM04520 cell | CLO_0018844 | [ TSC2 GENE; TSC2 TUBEROUS SCLEROSIS; TS] |
| GM16108 cell | CLO_0018845 | [ PALMITOYL-PROTEIN THIOESTERASE 1; PPT1 CEROID LIPOFUSCINOSIS, NEURONAL 1, INFANTILE; CLN1] |
| GM04518 cell | CLO_0018848 | [ MANNOSIDOSIS, ALPHA B, LYSOSOMAL] |
| GM04517 cell | CLO_0018849 | [ KRABBE DISEASE] |
| globoid cell leukodystrophy | DOID_10587 | |
| GM04534 cell | CLO_0018842 | [ HUNTINGTON DISEASE; HD] |
| GM04522 cell | CLO_0018843 | [ APPARENTLY HEALTHY FETAL TISSUE] |
| immortal human buttock-derived fibroblast cell line cell | CLO_0000684 | |
| ND06754 cell | CLO_0018840 | [ ASYMPTOMATIC AND GENETICALLY RELATED TO AN AFFECTED INDIVIDUAL EPILEPSY] |
| GM16109 cell | CLO_0018841 | [ CEROID LIPOFUSCINOSIS, NEURONAL 1, INFANTILE; CLN1 PALMITOYL-PROTEIN THIOESTERASE 1; PPT1] |
| IMG-679 cell | CLO_0006835 | |
| IMG-678 cell | CLO_0006834 | |
| IMG-676 cell | CLO_0006833 | |
| IMG-675 cell | CLO_0006832 |