All terms in DOID

Label Id Description
chest wall lipoma DOID_10200 [A thoracic benign neoplasm that derives_from fat cells and is located_in the chest wall.]
cervical Wilms' tumor DOID_5190 [A cervical carcinosarcoma is located_in the cervix with morphological features resembling Wilms tumor of the kidney.]
cervical carcinosarcoma DOID_4112 [A cervical cancer that has_material_basis_in carcinomatous (epithelial tissue) and sarcomatous (connective tissue) components.]
gallbladder lipoma DOID_10201 [A gallbladder benign neoplasm that is located_in the gallbladder and derives_from fat cells.]
nodular ganglioneuroblastoma DOID_5193
ganglioneuroblastoma DOID_4163
Abnormal nervous system morphology HP_0012639
obsolete non-neoplastic nevus of skin DOID_12860
obsolete recurrent nephroblastoma DOID_5184 [A nephroblastoma that recurs over time.]
hereditary Wilms' tumor DOID_5183 [A nephroblastoma that results_in either bilateral disease or a family history of Wilms' tumour.]
obsolete anaplastic renal Wilms' tumor DOID_5185 [A nephroblastoma that results_in an unfavorable appearance under the microscope. They are characterized by a cell nuclei that tends to be very large and distorted.]
chondroid lipoma DOID_10208 [A lipoma that is a deep-seated, firm, yellow tumors that characteristically occur on the legs of women.]
extrahepatic bile duct lipoma DOID_10209 [A biliary tract benign neoplasm that is located_in the extrahepatic bile duct and derives_from fat cells.]
lipoma of spermatic cord DOID_10206 [A paratesticular lipoma that is located_in the spermatic cord and derives_from fat cells.]
paratesticular lipoma DOID_10207 [A reproductive organ benign neoplasm that derives_from fat cells located_in the paratesticular region.]
epithelial predominant Wilms' tumor DOID_5189
reproductive organ benign neoplasm DOID_0050622 [An organ system benign neoplasm that is located_in reproductive system organs.]
lupus nephritis DOID_0080162 [A glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus.]
autosomal recessive autoinflammation, panniculitis, and dermatosis syndrome DOID_0080163 [An autoinflammation, panniculitis, and dermatosis syndrome characterized by neonatal onset of recurrent fever, erythematous rash with painful nodules, painful joints, and lipodystrophy and has_material_basis_in homozygous or compound heterozygous loss-of-function mutation in the OTULIN gene on chromosome 5p15.]
autoinflammation, panniculitis, and dermatosis syndrome DOID_0061170 [An autoinflammatory disease characterized by neonatal or infantile onset of systemic inflammation, fever, panniculitis, aseptic skin lesions, leukocytosis, neutrophilia, and elevated inflammatory markers, including C-reactive protein, with no overt primary immunodeficiency that has_material_basis_in mutation in the OTULIN gene on chromosome 5p15, that encodes a deubiquitinase with linear linkage specificity.]