All terms in DOID

Label Id Description
breast adenomyoepithelial adenosis DOID_7312
cocaine dependence DOID_9975 [A drug dependence that is a psychological dependency on the regular use of cocaine.]
drug dependence DOID_9974 [A substance dependence that involves the continued use of drugs despite problems related to use of the substance.]
substance dependence DOID_9973 [A substance-related disorder that involves the continued use of alcohol or other drugs despite problems related to use of the substance.]
gastroduodenitis DOID_8644
substance-related disorder DOID_303 [A disease of mental health involving the abuse or dependence on a substance that is ingested in order to produce a high, alter one's senses, or otherwise affect functioning.]
obsolete Hodgkin's paragranuloma involving lymph nodes of axilla and upper limb DOID_8641
Hodgkin's paragranuloma DOID_8642
hypervitaminosis A DOID_9972 [An overnutrition that is characterized by excess vitamin A, has_symptom hepatomegaly, anorexia, fever, alopecia, and arthralgia, and has_material_basis_in excessive intake of vitaimin A, and/or derangement of vitamin A metabolism.]
obsolete inherited neuropathy DOID_7316
acute female pelvic peritonitis DOID_9978
hallucinogen dependence DOID_9977 [A drug dependence that involves the continued use of hallucinogenic drugs despite problems related to use of the substance.]
subacute delirium DOID_8645
substance-induced psychosis DOID_8646
Jewett-Marshall bladder cancer DOID_7315
heroin dependence DOID_9976 [An opiate dependence that involves the continued use of heroin despite problems related to use of the substance.]
opiate dependence DOID_2559 [A drug dependence that involves the continued use of opiate drugs despite despite problems related to use of the substance.]
retroperitoneum carcinoma DOID_12342
amelogenesis imperfecta type 1F DOID_0110065 [An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the ameloblastin gene (AMBN) on chromosome 4q13.]
congenital dyserythropoietic anemia type I DOID_0111396 [A congenital dyserythropoietic anemia characterized by autosomal recessive inheritance of macrocytic anemia, ineffective erythropoiesis, and secondary hemochromatosis.]