Terminology Service for NFDI4Health
All terms in MESH
| Label | Id | Description |
|---|---|---|
| violacin A | C510720 | |
| Mg5 ceramic | C499885 | |
| trichoclin acetate | C510721 | |
| touchtone protein, zebrafish | C499886 | |
| Ze 450 | C510722 | |
| NCX 1022 | C499887 | |
| 4-(N-tert-butyloxyamino)-2-(methoxymethylenyl)pyridine | C510723 | |
| platinum(II) methionine dichloride | C510724 | |
| di-(5-((4-(4-butylphenyl)azo)phenoxy)pentyl)phosphate | C510725 | |
| Xmus101protein, Xenopus | C510726 | |
| (1,1'-4',1''-terphenyl)-4,4''-dimethanethiol | C510727 | |
| CHD9 protein, rat | C510728 | |
| 11-amino-1-undecanethiol | C510729 | |
| Hs1 pro-1 protein, Beta procumbens | C103918 | |
| Rps12 protein, plant | C103919 | |
| Chromosome Banding | D002871 | [Staining of bands, or chromosome segments, allowing the precise identification of individual chromosomes or parts of chromosomes. Applications include the determination of chromosome rearrangements in malformation syndromes and cancer, the chemistry of chromosome segments, chromosome changes during evolution, and, in conjunction with cell hybridization studies, chromosome mapping.] |
| Chromosome Deletion | D002872 | [Actual loss of portion of a chromosome.] |
| Loss of Heterozygosity | D019656 | [The loss of one allele at a specific locus, caused by a deletion mutation; or loss of a chromosome from a chromosome pair, resulting in abnormal HEMIZYGOSITY. It is detected when heterozygous markers for a locus appear monomorphic because one of the ALLELES was deleted.] |
| Monosomy | D009006 | [The condition in which one chromosome of a pair is missing. In a normally diploid cell it is represented symbolically as 2N-1.] |
| Sequence Deletion | D017384 | [Deletion of sequences of nucleic acids from the genetic material of an individual.] |