Terminology Service for NFDI4Health
All terms in CLO
| Label | Id | Description |
|---|---|---|
| WSU-NHL cell | CLO_0009636 | |
| WR19M.1 cell | CLO_0009630 | [disease: macrophage; AMLV-induced tumor] |
| WR21 cell | CLO_0009631 | |
| immortal mouse submandibular gland-derived cell line cell | CLO_0000898 | |
| WRC cell | CLO_0009632 | |
| GM09132 cell | CLO_0010622 | [ TRANSLOCATED CHROMOSOME] |
| GM09117 cell | CLO_0010623 | [ ORNITHINE AMINOTRANSFERASE DEFICIENCY] |
| GM08684 cell | CLO_0010620 | [ ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN; ACADM] |
| GM09118 cell | CLO_0010621 | [ ORNITHINE AMINOTRANSFERASE DEFICIENCY] |
| lysosomal storage disease | DOID_3211 | |
| glycogen storage disease type VI | DOID_2754 | |
| tic disorder | DOID_2769 | |
| movement disorder | DOID_480 | |
| vascular hemostatic disorder | DOID_484 | |
| epidermolysis bullosa | DOID_2730 | |
| vesiculobullous skin disease | DOID_2731 | |
| atrophic condition of skin | DOID_2733 | |
| hyperbilirubinemia | DOID_2740 | |
| hereditary hyperbilirubinemia | DOID_2741 | |
| intestinal junction | UBERON_8410024 |