All terms in DOID

Label Id Description
adolescence-adult electroclinical syndrome DOID_0050705 [An electroclinical syndrome with onset in adolescence and adulthood.]
obsolete hemophilia DOID_2230
middle ear carcinoma DOID_4893 [A middle ear cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells.]
middle ear cancer DOID_5099 [An ear cancer that is located_in the middle ear.]
middle ear adenocarcinoma DOID_4892 [A middle ear carcinoma that derives_from epithelial cells of glandular origin.]
factor XII deficiency DOID_2231 [A blood coagulation disease that is characterized by prolonged PTT time without clinical symptoms, and has_material_basis_in a mutation in the F12 gene on chromosome 5q33.]
obsolete coagulation factor deficiency DOID_2232
rete ovarii benign neoplasm DOID_4895 [A female reporoductive organ benign neoplasm that is located_in the rete ovarii.]
female reproductive organ benign neoplasm DOID_0060086 [A reproductive organ benign neoplasm that is characterized by a lack of malignancy located_in the female reproductive system.]
severe myalgia SYMP_0000379 [A muscle pain that is characterized by being severe in nature. Myalgia may be acute in nature, stemming from overuse of a muscle group or viral infection. It may also be chronic and caused by metabolic myopathy, some nutritional deficiencies, and chronic fatigue syndrome.]
rete ovarii adenocarcinoma DOID_4894 [An ovary adenocarcinoma that arises from the rete ovarii.]
obsolete partial epilepsy with impairment of consciousness DOID_2233
severe diarrhea SYMP_0000376
epilepsy DOID_1826 [A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.]
Severe acute respiratory syndrome coronavirus NCBITaxon_2901879
Severe acute respiratory syndrome-related coronavirus NCBITaxon_694009
prothrombin deficiency DOID_2235 [A thrombophilia that is characterized by bleeding symptoms due to low levels of circulating prothrombin, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the gene encoding coagulation factor II, also known as prothrombin, on chromosome 11p11.]
scrotal abscess SYMP_0000374 [A reproductive system symptom that is characterized by an abscess that is either superficial or intrascrotal. Superficial scrotal abscess may occur from an infected hair follicle, infection of a scrotal laceration, or minor scrotal surgery. Intrascrotal abscess most commonly arises from bacterial epididymitis, but may also be related to tuberculous infection of the epididymis, a testicular abscess that ruptures through the tunica albuginea, or drainage of appendicitis into scrotum through a patent processus vaginalis or as a result of extravasation of infected urine from the urethra in patients with a urethral stricture and neurogenic bladder using an external collection device.]
congenital afibrinogenemia DOID_2236 [A blood coagulation disease that is characterized by an impaired blood clotting resulting from a lack deficiency of a the fibrinogen protein (coagulation factor I).]
severe abdominal cramp SYMP_0000375