All terms in EFO
| Label | Id | Description |
|---|---|---|
| skeletal muscle tissue | UBERON_0001134 | [Muscle tissue that consists primarily of skeletal muscle fibers.] |
| lacrimal gland cancer | MONDO_0002464 | [A malignant neoplasm involving the lacrimal gland.] |
| lacrimal system cancer | MONDO_0002460 | [A cancer that involves the lacrimal apparatus.] |
| lacrimal gland neoplasm | MONDO_0021222 | [A neoplasm (disease) that involves the lacrimal gland.] |
| plant embryo | PO_0009009 | [A whole plant (PO:0000003) that participates in the plant embryo stage (PO:0007631).] |
| head mesenchyme from mesoderm | UBERON_0006904 | [A head mesenchyme that develops_from a mesoderm.] |
| nephritis | EFO_1002050 | [Inflammation of renal tissue. [ NCIt:P378 ], Inflammation of renal tissue.] |
| kidney failure | EFO_1002048 | [An acute or chronic condition that is characterized by the inability of the kidneys to adequately filter the blood., An acute or chronic condition that is characterized by the inability of the kidneys to adequately filter the blood. [ NCIt:P378 ]] |
| lacrimal gland carcinoma | MONDO_0002463 | [A carcinoma that arises from epithelial cells of the lacrimal gland.] |
| cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome | MONDO_0014455 | |
| Hennekam lymphangiectasia-lymphedema syndrome 2 | MONDO_0014454 | [Any Hennekam syndrome in which the cause of the disease is a mutation in the FAT4 gene.] |
| stamen | PO_0009029 | [A microsporophyll bearing one or more microsporangia.] |
| flower | PO_0009046 | [A determinate reproductive shoot system (PO:0025082) that has as part at least one carpel (PO:0009030) or at least one stamen (PO:0009029) and does not contain any other determinate shoot system (PO:0009006) as a part. [ POC:curators ] , The reproductive structure of the anthophyta or angiosperms.] |
| breasts and/or nipples, aplasia or hypoplasia of, 2 | MONDO_0014450 | [Any isolated congenital breast hypoplasia/aplasia in which the cause of the disease is a mutation in the PTPRF gene.] |
| isolated congenital breast hypoplasia/aplasia | MONDO_0015855 | |
| type II hypersensitivity | GO_0002445 | [An inflammatory response resulting in cell death or dysfunction mediated by activation of the classical complement pathway or induction of effector cell phagocytosis, cytolysis mechanisms via complement or Fc receptors following the binding of antibodies to cell surface antigens on a target cell, or mediated by the direct binding of antibody to cellular receptors.] |
| bursitis | MONDO_0002471 | [Inflammation or irritation of a synovial bursa, the fibrous sac that acts as a cushion between moving structures of bones, muscles, tendons or skin.] |
| synovial bursa disorder | MONDO_0056802 | [A disease or disorder that involves the synovial bursa.] |
| primary hyperoxaluria | MONDO_0002474 | [A hereditary disorder characterized by excessive oxalate production, leading to hyperoxaluria.] |
| Double outlet right ventricle with doubly committed ventricular septal defect | Orphanet_99047 |