All terms in EFO
| Label | Id | Description |
|---|---|---|
| Sg4 | EFO_0005839 | [Clone of S2. Differs from the S2 cell distributed by the DGRC in many transcriptional properties, among them a higher expression of Abd-B in Sg4, and a much higher expression of defensins in S2.] |
| Pyruvate kinase hyperactivity | EFO_0005840 | [Autosomal dominant phenotype characterized by increase of red blood cell ATP.] |
| cortisol measurement | EFO_0005843 | [quantification of the hormone cortisol in blood or urine] |
| obsolete_mucopolysaccharidosis type 2, attenuated form | Orphanet_217093 | |
| increased risk | EFO_0005847 | [An increase in the probability of an event occuring, as compared to a background risk such as the normal risk in a given population. For intsance, the increased risk of getting breast cancer given a Brca1 mutation.] |
| risk factor | EFO_0003919 | [An aspect of personal behavior or lifestyle, environmental exposure, or inborn or inherited characteristic, which, on the basis of epidemiologic evidence, is known to be associated with a health-related condition considered important to prevent., Any aspect of an individual's life, behavior, an environmental exposure, or an inborn or inherited characteristic that increases the likelihood of a disease, condition or injury.] |
| hemoglobin A2 measurement | EFO_0005845 | [Hemoglobin A2 measurement is a measure of the quantity of the metallo protein hemoglobin A2, a tetramer of alpha- and delta-globin chains, in blood, The determination of the amount of hemoglobin A2 present in a sample. [ NCI ]] |
| cryoglobulinemia | EFO_0005846 | [Cryoglobulinemia is a type of vasculitis that is caused by abnormal proteins (antibodies) in the blood called 'cryoglobulins.' At cold temperatures, these proteins become solid or gel-like, which can block blood vessels and cause a variety of health problems. Many people affected by this condition will not experience any unusual signs or symptoms. When present, symptoms vary but may include breathing problems; fatigue; glomerulonephritis ; joint or muscle pain; purpura ; Raynaud's phenomenon ; skin death; and/or skin ulcers. In some cases, the exact underlying cause is unknown; however, cryoglobulinemia can be associated with a variety of conditions including certain types of infection; chronic inflammatory diseases (such as autoimmune disease); and/or cancers of the blood or immune system. Treatment varies based on the severity of the condition, the symptoms present in each person and the underlying cause., A condition characterized by the presence of cryoglobulins in the blood. Cryoglobulins are abnormal proteins that precipitate within the microvasculature on exposure to cold; microvasculature effects of cryoglobulinemia may result in restricted tissue blood flow, tissue hypoxia, and tissue necrosis. --2004] |
| type IV hypersensitivity disease | MONDO_0002459 | [A disease that has its basis in the disruption of type IV hypersensitivity.] |
| ML-DmD21 | EFO_0005829 | [This cell line was derived from the third instar larval stage (y v f mal) of dorsal mesothoracic discs. The cells originated from the Miyake lab, and are male by criterion of roX expression (DGRC, unpublished).] |
| ML-DmD20-c2 | EFO_0005827 | [This cell line was derived from the third instar larval stage (y v f mal) of antennal discs. Originated from the Miyake lab and cloned from its parent ML-DMD20 cell line. Cells are male, by criterion of roX expression.] |
| ML-DmD20-c5 | EFO_0005828 | [This cell line was derived from the third instar larval stage (y v f mal) of antennal discs. Originated from the Miyake lab and cloned from its parent ML-DMD20 cell line. Cells are male, by criterion of roX expression.] |
| Mycobacterium smegmatis str. MC2 155 | NCBITaxon_246196 | |
| obsolete_porphyria due to ALA dehydratase deficiency | Orphanet_100924 | |
| apical ectodermal ridge pectoral fin bud | ZFA_0000085 | [Apical ectodermal ridge that is part of the pectoral fin bud.] |
| ML-DmD8 | EFO_0005832 | [This cell line was derived from the third instar larval stage (y v f mal) of dorsal mesothoracic discs. Originated from the Miyake lab.] |
| obsolete_mucopolysaccharidosis type 2, severe form | Orphanet_217085 | |
| ML-DmD9 | EFO_0005833 | [This cell line was derived from the third instar larval stage (y v f mal) of dorsal mesothoracic discs. Originated from the Miyake lab.] |
| ML-DmD32 | EFO_0005830 | [This cell line was derived from the third instar larval stage (y v f mal) of dorsal mesothoracic discs. Originated from the Miyake lab.] |
| ML-DmD4-c1 | EFO_0005831 | [This cell line was derived from the third instar larval stage (y v f mal) of imaginal discs. Originated from the Miyake lab and cloned from its parent ML-DMD4 cell line.] |