All terms in EFO
| Label | Id | Description |
|---|---|---|
| retinoic acid | CHEBI_26536 | [A retinoid that has formula C20H28O2.] |
| obsolete_race | EFO_0001432 | [An arbitrary classification of a taxonomic group that is a division of a species. It usually arises as a consequence of geographical isolation within a species and is characterized by shared heredity, physical attributes and behavior, and in the case of humans, by common history, nationality, or geographic distribution., A race is a popluation categorized on the basis of various sets of heritable characteristics.] |
| obsolete_Machado-Joseph disease type 2 | Orphanet_276241 | [Machado-Joseph disease type 2 is a subtype of Machado-Joseph disease (SCA3/MJD, see this term) with intermediate severity characterized by an intermediate age of onset, cerebellar ataxia and external progressive ophthalmoplegia, with variable pyramidal and extrapyramidal signs.] |
| obsolete_Machado-Joseph disease type 3 | Orphanet_276244 | [Machado-Joseph disease type 3 is a subtype of Machado-Joseph disease (SCA3/MJD, see this term) of milder severity characterized by late onset, slower progression, and peripheral amyotrophy.] |
| xylonate | CHEBI_27345 | |
| (-)-demecolcine | CHEBI_4393 | |
| obsolete_non-syndromic male infertility due to sperm motility disorder | Orphanet_276234 | |
| uninfected | EFO_0001460 | [Uninfected class is a disposition in which the bearer is not known to be affected by a disease withtin the context of a study] |
| obsolete_Machado-Joseph disease type 1 | Orphanet_276238 | [Machado-Joseph disease type 1 is a rare, usually severe subtype of Machado-Joseph disease (SCA3/MJD, see this term) characterized by the presence of marked pyramidal and extrapyramidal signs.] |
| obsolete_severe congenital neutropenia | Orphanet_42738 | |
| control | EFO_0001461 | [The act of directing or determining; regulation or maintenance of a function or action; a relation of constraint of one entity (thing or person or group) by another., A control role is borne by a material in a process in which results obtained from an experimental sample and a control sample are compared.] |
| obsolete_mucopolysaccharidosis type 6, slowly progressing | Orphanet_276223 | |
| Rhizobium etli CFN 42 | NCBITaxon_347834 | |
| Roseburia inulinivorans | NCBITaxon_360807 | |
| sucrose | CHEBI_17992 | [A glycosyl glycoside that has formula C12H22O11.] |
| obsolete_antibiotic | EFO_0001485 | [Substance produced by, and obtained from, certain living cells (especially bacteria, yeasts and moulds), or an equivalent synthetic substance, which is biostatic or biocidal at low concentrations to some other form of life, especially pathogenic or noxious organisms.] |
| aspartate(2-) | CHEBI_29995 | [A C4-dicarboxylate that is the dianion obtained by the deprotonation of both the carboxy groups of aspartic acid.] |
| desferrioxamine B | CHEBI_4356 | |
| obsolete_Hemihyperplasia-multiple lipomatosis syndrome | Orphanet_276280 | [Hemihyperplasia-multiple lipomatosis syndrome is a rare, genetic overgrowth syndrome characterized by non- progressive, asymmetrical, moderate hemihyperplasia (frequently affecting the limbs) associated with slow growing, painless, multiple, recurrent, subcutaneous lipomatous masses distributed throughout entire body (in particular back, torso, extremities, fingers, axillae). Superficial vascular malformations may also be associated. Increased risk of intra-abdominal embryonal malignancies may be associated.] |
| obsolete_PHACE syndrome | Orphanet_42775 |