All terms in EFO
| Label | Id | Description |
|---|---|---|
| N-formyl-L-methionine | CHEBI_16552 | [A L-methionine derivative in which one of the hydrogens attached to the nitrogen is replaced by a formyl group.] |
| CS57624 | EFO_0000040 | [CS57624 is an Arabidopsis thaliana strain as described in TAIR http://www.arabidopsis.org/servlets/TairObject?id=1005158648&type=germplasm] |
| CS57625 | EFO_0000041 | [CS57625 is an Arabidopsis thaliana strain as described in TAIR http://www.arabidopsis.org/servlets/TairObject?id=1005158649&type=germplasm] |
| CS57626 | EFO_0000042 | [CS57626 is an Arabidopsis thaliana strain as described in TAIR http://www.arabidopsis.org/servlets/TairObject?id=1005158650&type=germplasm] |
| CS57627 | EFO_0000043 | [CS57627 is an Arabidopsis thaliana strain as described in TAIR http://www.arabidopsis.org/servlets/TairObject?id=1005158651&type=germplasm] |
| CS57628 | EFO_0000044 | [CS57628 is an Arabidopsis thaliana strain as described in TAIR http://www.arabidopsis.org/servlets/TairObject?id=1005158652&type=germplasm] |
| CS57629 | EFO_0000045 | [CS57629 is an Arabidopsis thaliana strain as described in TAIR http://www.arabidopsis.org/servlets/TairObject?id=1005158653&type=germplasm] |
| CS57630 | EFO_0000046 | [CS57630 is an Arabidopsis thaliana strain as described in TAIR http://www.arabidopsis.org/servlets/TairObject?id=1005158654&type=germplasm] |
| CS57631 | EFO_0000047 | [CS57631 is an Arabidopsis thaliana strain as described in TAIR http://www.arabidopsis.org/servlets/TairObject?id=1005158655&type=germplasm] |
| CS57637 | EFO_0000048 | [CS57637 is an Arabidopsis thaliana strain as described in TAIR http://www.arabidopsis.org/servlets/TairObject?id=1005158661&type=germplasm] |
| Fragaria x ananassa | NCBITaxon_3747 | |
| CS57641 | EFO_0000049 | [CS57641 is an Arabidopsis thaliana strain as described in TAIR http://www.arabidopsis.org/servlets/TairObject?id=1005158665&type=germplasm] |
| obsolete_Familial renal amyloidosis due to Apolipoprotein AII variant | Orphanet_238269 | |
| obsolete_neonatal glycine encephalopathy | Orphanet_289857 | |
| (2,4-dichlorophenoxy)acetic acid | CHEBI_28854 | [A chlorophenoxyacetic acid that has formula C8H6Cl2O3., Encoded by HOXC6 Gene (ANTP Family), 153- and 235-amino acid (27-kD) Homeobox C6 Protein isoforms are highly conserved sequence-specific DNA-binding homeobox transcription repressors that can cooperate with other HOX proteins and may contribute to the breast cell phenotype through co-operative interactions. As part of a developmental regulatory system that provides anterior-posterior positional identity to cells, HOXC6 may regulate the coordinated expression of multiple genes involved in morphogenesis and differentiation. (from LocusLink, Swiss-Prot, OMIM, and NCI), Homeobox protein Hox-C6 (235 aa, ~27 kDa) is encoded by the human HOXC6 gene. This protein plays a role in transcription and embryonic development.] |
| Salmonella enterica subsp. enterica serovar Kentucky | NCBITaxon_192955 | |
| acute myeloid leukemia, der12p | MONDO_0100390 | [Any acute myeloid leukemia that has the chromosomal anomaly der12p. (A cytogenetic abnormality involving the rearrangement of two or more other chromosomes with the short arm of chromosome 12 (12p).)] |
| acute myeloid leukemia, t(2;12) | MONDO_0100391 | [Any acute myeloid leukemia that has the chromosomal anomaly t(2;12). (A cytogenetic abnormality that involves a translocation between chromosomes 2 and 12.)] |
| acute myeloid leukemia, t(11;17) | MONDO_0100392 | [Any acute myeloid leukemia that has the chromosomal anomaly t(11;17). (A cytogenetic abnormality that involves a translocation between chromosomes 11 and 17.)] |
| acute myeloid leukemia, t(8;16) | MONDO_0100393 | [Any acute myeloid leukemia that has the chromosomal anomaly t(8;16). (A cytogenetic abnormality that involves a translocation between chromosomes 8 and 16.)] |