All terms in EFO
| Label | Id | Description |
|---|---|---|
| serum lipase activity measurement | EFO_0005849 | [quantification of some lipase activity in blood. It is used as a diagnostic test for pancreatitis, pancreatic cancer and and in the diagnosis and monitoring of coelic disease, Chrohn's disease and cystic fibrosis.] |
| enzyme | OBI_0000427 | [(protein or rna) or has_part (protein or rna) and has_function some GO:0003824 (catalytic activity), (protein or rna) or has_part (protein or rna) and has_function some GO:0003824 (catalytic activity)] |
| organic substance biosynthetic process | GO_1901576 | [ The chemical reactions and pathways resulting in the formation of an organic substance, any molecular entity containing carbon. ] |
| oligogalacturonide | CHEBI_62533 | |
| caudal ganglionic eminence | UBERON_0004026 | [The caudally located, distinct elevation of a transient proliferating cell mass of the fetal subventricular zone, located adjacent to the lateral ventricle.] |
| emphysema pattern measurement | EFO_0005850 | [quantification by computed tomography scans of distinct pathologic patterns in the lungs that occur in emphysema] |
| emphysema imaging measurement | EFO_0007626 | [Quantification of some aspect, eg the presence/absence or severity of emphysema through the use of imaging techniques such as CT scans] |
| electroclinical syndrome | MONDO_0000411 | [An epilepsy syndrome that is a group of clinical entities showing a cluster of electro-clinical characteristics, classified according to age at onset, cognitive and developmental antecedents and consequences, motor and sensory examinations, EEG features, provoking or triggering factors, and patterns of seizure occurrence with respect to sleep.] |
| height-adjusted body mass index | EFO_0005851 | [height-adjusted version of BMI calculated as BMI[x] = weight(kg)/height(m)^x), where x is derived to give the lowest Pearson's correlation coefficient of BMI[x] with height within a study cohort] |
| allergic rhinitis | EFO_0005854 | [Inflammation of the nasal mucous membranes caused by an IgE-mediated response to external allergens. The inflammation may also involve the mucous membranes of the sinuses, eyes, middle ear, and pharynx. Symptoms include sneezing, nasal congestion, rhinorrhea, and itching. It may lead to fatigue, drowsiness, and malaise thus causing impairment of the quality of life.] |
| narcolepsy without cataplexy | EFO_0005855 | [Narcolepsy without cataplexy is characterized by excessive day-time sleepiness associated with uncontrollable sleep urges and sometimes paralysis at sleep, hypnagogic hallucinations and automatic behavior., A condition characterized by recurrent episodes of daytime somnolence and lapses in consciousness (microsomnias). People who have narcolepsy without cataplexy have sleepiness but no emotionally triggered muscle weakness, and generally have less severe symptoms. ] |
| Heschl's gyrus morphology measurement | EFO_0005852 | [quantification of the morphology (eg thickness and surface area) of Heschl's gyrus, a core region of the auditory cortex with highly variable morphology] |
| response to silica exposure | EFO_0005853 | [short or long term physiological response of an organism, eg in terms of deposits of silica particles in lung tissues, to exposure to silica, usually of occupational or environment origin] |
| C. elegans embryo stage | EFO_0005858 | [The whole period of embryogenesis, from the formation of an egg till its hatch. [ http://www.wormbase.org/db/gene/gene?name=wjc ] ] |
| embryo stage | EFO_0007725 | [A life cycle stage that starts with fertilization and ends with the fully formed embryo.] |
| Caenorhabditis elegans | NCBITaxon_6239 | |
| bone inflammation disease | MONDO_0002614 | [Inflammation of the bone.] |
| mouse embryo stage | EFO_0005857 | [An embryo stage for the mouse species.] |
| mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type) | MONDO_0014820 | [Any mitochondrial DNA depletion syndrome in which the cause of the disease is a mutation in the OPA1 gene.] |
| 15q14 microdeletion syndrome | MONDO_0014822 | [15q14 microdeletion syndrome is a recently described syndrome characterized by developmental delay, short stature and facial dysmorphism.] |