All terms in EFO
| Label | Id | Description |
|---|---|---|
| childhood acute myeloid leukemia | EFO_0000330 | [Acute myeloid leukemia occurring in childhood.] |
| childhood leukemia | MONDO_0004355 | [An acute or chronic leukemia that occurs during childhood.] |
| ILSXISS80/TejJ | EFO_0002993 | |
| ribose phosphate biosynthetic process | GO_0046390 | [ The chemical reactions and pathways resulting in the formation of ribose phosphate, any phosphorylated ribose sugar. ] |
| organophosphate biosynthetic process | GO_0090407 | [ The chemical reactions and pathways resulting in the biosynthesis of deoxyribose phosphate, the phosphorylated sugar 2-deoxy-erythro-pentose. ] |
| carbohydrate derivative biosynthetic process | GO_1901137 | [ The chemical reactions and pathways resulting in the formation of carbohydrate derivative. ] |
| ILSXISS79/TejJ | EFO_0002992 | |
| chondroblastoma | EFO_0000331 | [A benign, chondroid-producing, well-circumscribed, lytic neoplasm usually arising from the epiphysis of long bones. It is characterized by the presence of chondroblasts, osteoclast-like giant cells, chondroid formation, calcification, and mitotic activity. In aggressive cases, there is rearrangement of the 8q21 chromosome band. It occurs most frequently in children and young adults and rarely metastasizes.] |
| benign chondrogenic neoplasm | MONDO_0024470 | [A non-metastasizing cartilaginous matrix-producing neoplasm characterized by the presence of neoplastic chondrocytes. Representative examples include osteochondroma and chondroma.] |
| chondromyxoid fibroma | EFO_0000332 | [An uncommon benign cartilaginous neoplasm arising from the bone. It is characterized by the presence of spindle-shaped or stellate chondrocytes, a lobulated growth pattern, myxoid stroma formation, and sometimes multinucleated giant cells. It has been associated with chromosomal rearrangement of 6q13 and 6q25 bands. The most common clinical symptom is mild, localized pain.] |
| ILSXISS86/TejJ | EFO_0002995 | |
| ILSXISS84/TejJ | EFO_0002994 | |
| chondrosarcoma | EFO_0000333 | [A malignant cartilaginous matrix-producing mesenchymal neoplasm arising from the bone and soft tissue. It usually affects middle-aged to elderly adults. The pelvic bones, ribs, shoulder girdle, and long bones are the most common sites of involvement. Most chondrosarcomas arise de novo, but some may develop in a preexisting benign cartilaginous lesion.] |
| obsolete_chordoma | EFO_0000334 | [A malignant tumor arising from the embryonic remains of the notochord. It is also called chordocarcinoma, chordoepithelioma, and notochordoma. (Dorland, 27th ed), A notochordal cancer that derives_from cellular remnants of the notochord., A malignant bone tumor arising from the remnants of the fetal notochord. Although it can occur at all ages, it is more frequently seen in middle-aged adults. Most frequent sites of involvement are: sacrococcygeal area, spheno-occipital area, and the cervico-thoraco-lumbar spine. Microscopically, chordomas are composed of cells that form cords and lobules, separated by mucoid intercellular tissue. Some of the cells are large (physaliphorous) and have vacuolated cytoplasm and prominent vesicular nuclei. Other tumor cells are small with small nuclei without visible nucleoli. Chordomas tend to recur and may metastasize. The most common sites of metastasis are skin and bone.] |
| ILSXISS90/TejJ | EFO_0002997 | |
| ILSXISS89/TejJ | EFO_0002996 | |
| chromophobe renal cell carcinoma | EFO_0000335 | [Chromophobe renal cell carcinoma is a rare subtype of renal cell carcinoma, originating from the intercalating cells of the collecting ducts and macroscopically manifesting as a well-circumscribed, highly lobulated, solid tumor that is usually diagnosed at an early stage. It is frequently asymptomatic, or may present with nonspecific symptoms, such as weight loss, fever or fatigue. The classic presentation observed in renal tumors (hematuria, flank pain and palpable mass) is occasionally observed and usually indicates an advanced stage of the disease. It is most frequently sporadic however, several familial cases, associated with Birt-Hogg DubC) syndrome, have been described.] |
| genetic modification | EFO_0000510 | [A genetic modification of the genome of an organism which may occur naturally by spontaneous mutation, or be introduced by some experimental means. Examples of genetic modification include specification of a transgene or the gene knocked-out or details of transient transfection.] |
| ILSXISS94/TejJ | EFO_0002999 | |
| ILSXISS92/TejJ | EFO_0002998 |