Terminology Service for NFDI4Health
All terms in CLO
| Label | Id | Description |
|---|---|---|
| M-G93 cell | CLO_0007701 | |
| MH1 cell | CLO_0007708 | [disease: hybridoma] |
| MH subscript(1) C subscript(1) cell | CLO_0007707 | [disease: hepatoma] |
| mh cell | CLO_0007706 | [disease: Hermansky-Pudlak syndrome] |
| MGP96Na cell | CLO_0007705 | |
| alkaptonuria | DOID_9270 | |
| inborn errors of amino acid metabolism | DOID_9252 | |
| hyperlysinemia | DOID_9274 | |
| inborn metabolic brain disease | DOID_889 | |
| M-G89 cell | CLO_0007700 | |
| inborn urea cycle disorder | DOID_9267 | |
| ciliary plasm | GO_0097014 | [Note that we deem cilium and microtubule-based flagellum to be equivalent. Also, researchers consider the composition of both the plasm and the membrane of the cilium to be detectably different from that in the non-ciliary cytosol and plasma membrane (e.g. in terms of calcium ion concentration, membrane lipid composition, and more). For this reason, the term "ciliary plasm" is not linked to "cytoplasm".] |
| cystinuria | DOID_9266 | |
| amino acid transport disorder | DOID_1058 | |
| renal minoaciduria | DOID_1061 | |
| sulfuraminoacidemia | DOID_9264 | |
| disturbance of metabolism of leucine, isoleucine and valine | DOID_858 | |
| nonketotic hyperglycinemia | DOID_9268 | |
| MH1C1 cell | CLO_0007709 | [disease: hepatoma] |
| MHH-CALL-2 cell | CLO_0007715 |