All terms in DOID

Label Id Description
obsolete ovarian serous tumor DOID_6213
obsolete recurrent esophagus cancer DOID_7544
bladder diffuse clear cell adenocarcinoma DOID_6210
bladder clear cell adenocarcinoma DOID_5306 [A clear cell adenocarcinoma that is located_in the bladder.]
mixed epithelial/mesenchymal metaplastic breast carcinoma DOID_7541 [A breast metaplastic carcinoma that is characterized by the presence of epithelial and mesenchymal components.]
susceptibility to systemic lupus erythematosus 1 MIM_601744
mixed epithelial tumor of ovary DOID_6211 [An ovarian benign neoplasm that is biphasic and has_material_basis_in epithelial and mesenchymal elements.]
osteosarcoma arising in bone Paget's disease DOID_7542
penis carcinoma in situ DOID_8872 [An in situ carcinoma that is located_in the penis.]
penile disease DOID_1529
otitis SYMP_0000873 [Otitis is a ear symptom characterized as a general term for inflammation or infection of the ear, in both humans and other animals.]
hematoma SYMP_0000874 [A skin and integumentary tissue symptom that is characterized by a mass of usually clotted blood that forms in a tissue, organ, or body space as a result of a broken blood vessel generally the result of hemorrhage, or more specifically, internal bleeding.]
icteric mucous membrane SYMP_0000871 [A skin and integumentary tissue symptom that is characterized by yellowed mucous membranes due to bile or bilirubin accumulation.]
obsolete X-linked dominant disease DOID_0080340
icteric skin SYMP_0000872 [A skin and integumentary tissue symptom that is characterized by yellowed skin due to bile or bilirubin accumulation.]
obsolete herpetic vulvovaginitis DOID_8876 [A genital herpes that results_in infection located_in vulva and located_in vagina, has_material_basis_in Human herpesvirus 1 or Human herpesvirus 2 and has_symptom fever, has_symptom lymphadenopathy, and has_symptom lesions.]
obsolete X-linked recessive disease DOID_0080341
icteric eyes SYMP_0000870 [Icteric eyes is a eye symptom characterized by yellowed eyes due to bile or bilirubin accumulation.]
ceruminoma DOID_7549
mitochondrial complex IV deficiency nuclear type 2 DOID_0080357 [A COX deficiency, infantile mitochondrial myopathy that has_material_basis_in compound heterozygous mutation in the SCO2 gene on chromosome 22q13.]