Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
Actinomycetaceae	NCBITaxon_2049
Actinomycetales	NCBITaxon_2037
internal auditory canal lipoma	DOID_6752	[An auditory system benign neoplasm that derives_from adipose tissue and is located_in the internal auditory canal.]
lung combined type small cell carcinoma	DOID_5421	[A lung small cell carcinoma that is characterized as a multiphasic lung cancer comprised of a mixture of small cell and non-small cell lung carcinoma cells.]
lung small cell carcinoma	DOID_5409	[A lung carcinoma that has_material_basis_in primitive-appearing cells that are smaller than normal cells and is located_in the lung.]
obsolete malignant fibrous histiocytoma recurrent	DOID_6750
amyloid tumor	DOID_6755
obsolete central nervous system hemangioblastoma	DOID_5423
obsolete combined carcinoma of lung	DOID_5422
ovarian hyperstimulation syndrome	DOID_5425	[An ovarian disease that is characterized by cystic enlargement of the ovaries and a fluid shift from the intravascular to the third space and has_symptom abdominal pain, has_symptom nausea and has_symptom vomiting. This disease is an iatrogenic complication of assisted reproduction technology.]
bone lymphoma	DOID_6759	[A bone cancer and lymphoma by site that results_in lymphoma starting in the bone.]
urinary bladder villous adenoma	DOID_5427
premature ovarian failure	DOID_5426	[An ovarian disease where ovaries do not produce estrogen despite high levels of circulating gonadotropins in women under 40.]
bladder flat intraepithelial lesion	DOID_5429
Carney-Stratakis syndrome	DOID_0080533	[A syndrome that is characterized by the presence of multicentric paragangliomas and multifocal gastrointestinal stromal sarcoma tumors.]
myxofibrosarcoma	DOID_0080534	[A sarcoma that arises from the soft tissue and is characterized by the presence of spindle-shaped cells, cellular pleomorphism, thin-walled blood vessels, fibrous septa, and myxoid stroma.]
hypermanganesemia with dystonia	DOID_0080535	[A metal metabolism disorder that is characterized by involuntary, sustained muscle contractions (dystonia) and other uncontrolled movements resulting from excessive accumulation of manganese.]
hypermanganesemia with dystonia 1	DOID_0080536	[A hypermanganesemia with dystonia that is characterized by increased serum manganese, motor neurodegeneration with extrapyramidal features, polycythemia, and hepatic dysfunction and has_material_basis_in homozygous mutation in the SLC30A10 gene on chromosome 1q41.]
granular corneal dystrophy 1	DOID_0080530	[A granular corneal dystrophy that is characterized by recurrent erosions and gray crumb-like opacification located_in the cornea, proteinaceous rock candy-like deposits in the anterior stroma and subepithelium, and progressive vision loss later in life as deposits move into the central vision, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation of transforming growth factor beta-induced gene located in chromosome 5q31.1, which encodes keratoepithelin. Abnormalities lead to increased protein deposition and disruption of the corneal surface.]
dedifferentiated liposarcoma	DOID_0080531	[A liposarcoma that is characterized as a high-grade tumor that occurs when a lower-grade tumor changes and creates new high-grade cells.]