All terms in DOID

Label Id Description
Galloway-Mowat syndrome 4 DOID_0080246 [A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TP53RK gene on chromosome 20q13.]
obsolete intrathoracic lymph node tuberculosis DOID_11699 [A lymph node tuberculosis that is characterized by a peri-hilar or paratracheal lymph adenopathy after the primary infection. The diseased lymph nodes and associated inflammatory edema compress the airways resulting in partial or total airway obstruction. When a caseating lymph node erupts into an airway, aspiration of caseous material results in dense alveolar consolidation of the affected segment/lobe.]
obsolete metastatic tumor to the epididymis DOID_10367
Teleostomi NCBITaxon_117570
epididymis adenocarcinoma DOID_10368 [An epididymis cancer that derives_from epithelial cells of glandular origin.]
epididymis cancer DOID_10366 [A male reproductive organ cancer that is located in the epididymis.]
Functional abnormality of the gastrointestinal tract HP_0012719
obsolete chronic hypomanic disorder DOID_11696
portal vein thrombosis DOID_11695 [A hepatic vascular disease that is characterized by a blood clot that forms within the hepatic portal vein.]
contagious pustular dermatitis DOID_8771 [A viral infectious disease that results_in infection located_in skin, has_material_basis_in Orf virus (Parapoxvirus orf), which is transmitted_by contact with infected or recently vaccinated animals, or transmitted_by fomites carrying the virus. The infection has_symptom lesions on the finger, hand, arm, face, and penis.]
jugular foramen meningioma DOID_6110
chronic metabolic polyneuropathy DOID_7441
chronic polyneuropathy DOID_5221
obsolete reticulosarcoma involving intra-abdominal lymph nodes DOID_8770
obsolete diffuse intraductal papillomatosis DOID_7444
intracerebral cystic meningioma DOID_6113
obsolete ulcerative proctosigmoiditis DOID_8775
cerebral convexity meningioma DOID_6114
obsolete jugular foramen neoplasm DOID_6111
monoclonal gammopathy of uncertain significance DOID_7442 [A blood protein disease that is characterized by the presence of an abnormal protein called monoclonal protein in the blood.]