Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
trabecular follicular adenocarcinoma	DOID_3964
obsolete HIV encephalopathy	DOID_1306	[An acquired immunodeficiency syndrome that results_in infection located_in brain, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2. The infection has_symptom cognitive impairment, has_symptom motor dysfunction, and has_symptom behavioral change.]
cystadenoma	DOID_2634	[An adenoma that forms a cyst.]
Merkel cell carcinoma	DOID_3965
obsolete AIDS dementia complex	DOID_1305	[A HIV encephalopathy that results_in infection in adults located_in brain, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2. The infection has_symptom cognitive impairment, has_symptom motor dysfunction, has_symptom behavioral change, and has_symptom speech problems.]
obsolete mucinous neoplasm	DOID_2635
parachordoma	DOID_2647
cardiomyopathy	DOID_0050700	[A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle.]
obsolete wasting syndrome	DOID_1314
sebaceous adenoma	DOID_2648
Onchocerca	NCBITaxon_6281
aspartylglucosaminuria	DOID_0050461	[A lysosomal storage disease that is characterized by delayed speech at 2-3 years of age, has_material_basis_in mutations in the AGA gene that result in the absence or shortage of the aspartylglucosaminidase enzyme in lysosomes, preventing the normal breakdown of glycoproteins.]
obsolete HIV wasting syndrome	DOID_1313	[An acquired immunodeficiency syndrome that results_in involuntary loss of more than 10% of body weight, plus more than 30 days of either diarrhea, or weakness and fever, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2.]
chondroblastoma	DOID_2649	[A connective tissue benign neoplasm that derives_from chondroblasts and begins in cartilage at the ends of long bones (thighbone, shinbone, humerus) close to the joints.]
Wolf-Hirschhorn syndrome	DOID_0050460	[A chromosomal deletion syndrome that is characterized by distinct craniofacial features, hypotonia and intellectual disability and has_material_basis_in a microdeletion of the short arm of chromosome 4.]
glomerulosclerosis	DOID_0050851	[A glomerulonephritis that is characterized by hardening of the glomerulus in the kidney.]
campomelic dysplasia	DOID_0050463	[An osteochondrodysplasia that has_material_basis_in a mutation in chromosome 17 which results_in bowing in the located_in tibia or located_in femur.]
obsolete HIV-associated nephropathy	DOID_1311	[A renal infectious disease and is_a Human immunodeficiency virus infectious disease that results_in infection located_in kidney, has_material_basis_in has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2. The infection has_symptom nephrotic-range proteinuria (>3.5 g/d), has_symptom azotemia, has_symptom hypoalbuminemia, and has_symptom hyperlipidemia.]
Antley-Bixler syndrome	DOID_0050462	[A syndrome that is characterized at birth or prenatally by malformations and deformities affecting the majority of the skeleton and other areas of the body with autosomal recessive inheritance of the FGFR2 gene.]
Muir-Torre syndrome	DOID_0050465	[A Lynch syndrome that is characterized by a propensity to develop cancers of the gastrointestinal tract, genitourinary tract, and skin that has_material_basis_in mutations in DNA mismatch repair genes.]