Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
breast fibroadenosis	DOID_10352	[A breast benign neoplasm that has_material_basis in fibrous tissue and epithelial tissue in which tumor cells form glands or glandlike structures.]
pulmonary consolidation	SYMP_0000729
fibrosclerosis of breast	DOID_10353	[A non-proliferative fibrocystic change of the breast that contains scar tissue.]
obsolete glaucoma associated with systemic syndromes	DOID_11683
obsolete recurrent malignant pleural mesothelioma	DOID_7473
malignant pleural mesothelioma	DOID_7474	[A pleural cancer that has_material_basis_in mesothelium cells.]
respiratory system cancer	DOID_0050615	[An organ system cancer located_in the respiratory system that is characterized by uncontrolled cellular proliferation in the respiratory tract.]
mesothelial cell	CL_0000077
obsolete deep penetrating nevus	DOID_7471
obsolete recurrent nevus	DOID_7472
diverticulitis	DOID_7475	[An intestinal disease characterized by the formation and inflammation of diverticula within the bowel wall.]
nephrotic syndrome type 16	DOID_0080272	[A familial nephrotic syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the KANK2 gene on chromosome 19p13.]
microangiopathic hemolytic anemia	SYMP_0000720
polycystic kidney disease 5	DOID_0080273	[A autosomal recessive polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of homozygous mutation in the DZIP1L gene on chromosome 3q22.]
nasal cavity carcinoma in situ	DOID_6148	[An in situ carcinoma that is located_in the nasal cavity.]
duodenal somatostatinoma	DOID_7479
duodenum cancer	DOID_10021	[A small intestine cancer that is located_in the beginning section of the small intestine.]
multiple mitochondrial dysfunctions syndrome 5	DOID_0080274	[A multiple mitochondrial dysfunctions syndrome that is characterized by progressive neurologic deterioration beginning in early infancy, with affected individuals having no psychomotor development and early-onset seizures with neurologic decline and spasticity, and has_material_basis_in autosomal recessive inheritance of homozygous mutation in the iron-sulfur cluster assembly 1 gene on chromosome 9q21.]
Joubert syndrome 30	DOID_0080275
Neoplasm by anatomical site	HP_0011793	[Neoplasm categorized according to the anatomical site of origin of the neoplasm.]