All terms in DOID
| Label | Id | Description |
|---|---|---|
| cellular myxoid liposarcoma | DOID_5692 | |
| epithelioid cell melanoma | DOID_4360 | |
| visual cortex disease | DOID_5691 | |
| visual pathway disease | DOID_1393 | [An eye disease that affects the neural pathway from the optic nerve to the visual cortex, through which light is interpreted as an image.] |
| esophagus liposarcoma | DOID_5694 | |
| esophagus sarcoma | DOID_1114 | [An esophageal cancer that arises from transformed cells of mesenchymal origin sarcoma and located_in the esophagus.] |
| esophagus | UBERON_0001043 | |
| cervix disease | DOID_2253 | [A uterine disease that is located_in the cervix.] |
| adult liposarcoma | DOID_5693 | |
| colon signet ring adenocarcinoma | DOID_3033 | |
| larynx liposarcoma | DOID_5696 | [A liposarcoma that is located_in the larynx.] |
| Trichomonas vaginalis | NCBITaxon_5722 | |
| malignant breast melanoma | DOID_4364 | [A breast cancer that arises_from melanocytes.] |
| pediatric liposarcoma | DOID_5695 | |
| Trichomonadidae | NCBITaxon_181550 | |
| apparent mineralocorticoid excess syndrome | DOID_4367 | [A steroid inherited metabolic disorder characterized by decreased conversion of biologically active cortisol to inactive cortisone resulting in low aldosterone levels, metabolic alkalosis, hypernatremia, hypokalemia and early-onset severe hypertension that has_material_basis_in homozygous or compound heterozygous mutation in the HSD11B2 gene on chromosome 16.] |
| steroid inherited metabolic disorder | DOID_1701 | [A lipid metabolism disorder that involves defects in steroid metabolism.] |
| fibroblastic liposarcoma | DOID_5698 | |
| liposarcoma of the ovary | DOID_5697 | [An ovary sarcoma that arises from fatty tissue.] |
| obsolete brain hypoxia-Ischemia | DOID_4369 |