Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
(2-hydroxyphenyl)acetate	CHEBI_62423	[The monocarboxylic acid anion formed from (2-hydroxyphenyl)acetic acid by loss of a proton from the carboxy group; major microspecies at pH 7.3.]
lymphatic part of lymphoid system	UBERON_0006558	[An organ system subdivision that is a network of vessels capable of removing accumulating protein and fluid from the interstitial space and returning it to the vascular space. In some species, this network is connected to the immune system via lymph nodes and lymphocyte-producing organs, with the whole being the lymphoid system.]
lymphoid system	UBERON_0002465	[The lymphatic system in vertebrates is a network of conduits that carry a clear fluid called lymph. It also includes the lymphoid tissue through which the lymph travels. Lymphoid tissue is found in many organs, particularly the lymph nodes, and in the lymphoid follicles associated with the digestive system such as the tonsils. The system also includes all the structures dedicated to the circulation and production of lymphocytes, which includes the spleen, thymus, bone marrow and the lymphoid tissue associated with the digestive system[WP].]
toxicity	EFO_0011061	[The degree to which an agent can damage an organism.]
CME-W2	EFO_0005744	[The line was made from L3 prothoracic leg discs in the Milner lab (Currie et al., 1988).]
developmental and epileptic encephalopathy, 41	MONDO_0014916	[Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SLC1A2 gene.]
ventral wall of dorsal aorta	UBERON_0018549	[Region where blood progenitor markers are expressed. Probable site of definitive hematopoiesis between 36hpf and 4dpf.]
fGS/OSS	EFO_0005745	[This stable cell line is a mix of female germ-line stem cells/ovarian somatic sheet, which contains both germ-line and somatic cells.]
lung fibroblast derived cell line	EFO_0005742
Dias-Logan syndrome	MONDO_0014914	[Any BAFopathy in which the cause of the disease is a mutation in the BCL11A gene.]
BAFopathy	MONDO_0700120	[Disorder caused by mutations in the various subunits composing the BAF complex.]
obsolete_progressive retinal dystrophy due to retinol transport defect	Orphanet_352718
CME-W1-Cl.8+	EFO_0005743	[This cell line was cloned from CME W1 in the Milner lab. The line was derived from L3 dorsal mesothoracic disc (Currie et al., 1988). Transcriptome analysis suggests similarity to cells along the A/P boundary of the wing blade primordium, possibly at the D/V boundary (Cherbas et al., 2011). The sex is male, based on roX expression - (L. Cherbas).]
sessile serrated polyposis cancer syndrome	MONDO_0014919
hyperplastic polyposis syndrome	MONDO_0015524	[Hyperplastic polyposis syndrome is a rare, genetic intestinal disease characterized by the presence of multiple (usually large) hyperplastic/serrated colorectal polyps, usually with a pancolonic distribution. Histology reveals hyperplastic polyps, sessile serrated adenomas (most common), traditional serrated adenomas or mixed polyps. It is associated with an increased personal and familial (first-degree relatives) risk of colorectal cancer.]
G2	EFO_0005746	[Cells are made by W. Gehring from 6-10 hr embryos of cross y w f x In(3LR)C269, e mwh]
GM2	EFO_0005747	[Cells are of embryonic line made by Mosna and Dolfini. GM2 line was characterized by XO cells showing two “new” telocentric chromosomes while an autosome of the II pair was missing (Mosna and Dolfini, 1972). XO Drosophila are sterile males (http://www.ncbi.nlm.nih.gov/books/NBK10025/).]
obsolete_attenuated Chédiak-Higashi syndrome	Orphanet_352723
obsolete_X-linked sideroblastic anemia	Orphanet_75563	[X-linked sideroblastic anemia is a constitutional microcytic, hypochromic anemia of varying severity that is clinically characterized by manifestations of anemia and iron overload and that may respond to treatment with pyridoxine and folic acid.]
bronchial epithelial cell derived cell line	EFO_0005728	[A cell line derived from airway epithelial cells.]