All terms in CLO
| Label | Id | Description |
|---|---|---|
| GM05400 cell | CLO_0024821 | [ APPARENTLY HEALTHY NON-FETAL TISSUE] |
| GM18542 cell | CLO_0024822 | [ INTERNATIONAL HAPMAP PROJECT - JAPANESE IN TOKYO AND HAN CHINESE IN BEIJING (PLATE I) INTERNATIONAL HAPMAP PROJECT - HAN CHINESE IN BEIJING, CHINA CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 19; CYP2C19] |
| GM18544 cell | CLO_0024820 | [ INTERNATIONAL HAPMAP PROJECT - JAPANESE IN TOKYO AND HAN CHINESE IN BEIJING (PLATE II) INTERNATIONAL HAPMAP PROJECT - HAN CHINESE IN BEIJING, CHINA] |
| DA01156 cell | CLO_0024829 | [ DIABETES MELLITUS FAMILY SAMPLE] |
| DA01158 cell | CLO_0024827 | [ DIABETES MELLITUS FAMILY SAMPLE] |
| DA01155 cell | CLO_0024828 | [ DIABETES MELLITUS FAMILY SAMPLE] |
| GM05401 cell | CLO_0024825 | [ TRANSLOCATED CHROMOSOME DIGEORGE SYNDROME; DGS] |
| DA01157 cell | CLO_0024826 | [ DIABETES MELLITUS FAMILY SAMPLE] |
| GM02921 cell | CLO_0012834 | [ NEURAMINIDASE DEFICIENCY] |
| GM07056 cell | CLO_0036801 | [ CEPH/UTAH PEDIGREE 1340 INTERNATIONAL HAPMAP PROJECT - CEPH (PLATE I) [UTAH RESIDENTS WITH ANCESTRY FROM NORTHERN AND WESTERN EUROPE] CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 19; CYP2C19] |
| GM07057 cell | CLO_0036800 | [ SNP500 PANEL CEPH/UTAH PEDIGREE 1331] |
| GM02922 cell | CLO_0012833 | [ NEURAMINIDASE DEFICIENCY] |
| GM07054 cell | CLO_0036803 | [ CEPH/UTAH PEDIGREE 13294] |
| GM02923 cell | CLO_0012832 | [ NEURAMINIDASE DEFICIENCY] |
| GM07055 cell | CLO_0036802 | [ CEPH/UTAH PEDIGREE 1341 INTERNATIONAL HAPMAP PROJECT - CEPH (PLATE I) [UTAH RESIDENTS WITH ANCESTRY FROM NORTHERN AND WESTERN EUROPE] CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 19; CYP2C19] |
| GM02927 cell | CLO_0012831 | [ TRANSLOCATED CHROMOSOME] |
| GM02931 cell | CLO_0012830 | [ N-ACETYLGLUCOSAMINIDASE, ALPHA-; NAGLU MUCOPOLYSACCHARIDOSIS TYPE IIIB] |
| immortal Yellow baboon skin-derived fibroblast cell line cell | CLO_0000860 | |
| immortal blue monkey skin-derived fibroblast cell line cell | CLO_0000862 | |
| GM13395 cell | CLO_0012849 | [ HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY] |