Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
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.]
amelogenesis imperfecta type 1G	DOID_0110066	[An amelogenesis imperfecta that has_material_basis_in homozygous or compound heterozygous mutation in the FAM20A gene on chromosome 17q24.]
congenital dyserythropoietic anemia type Ib	DOID_0111397	[A congenital dyserythropoietic anemia type I that has_material_basis_in homozygous or compound heterozygous mutation in C15orf41 on chromosome 15q14.]
amelogenesis imperfecta hypomaturation type 2A5	DOID_0110063	[An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the SLC24A4 gene on chromosome 14q32.]