Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
Listeria	NCBITaxon_1637
gallbladder leiomyoma	DOID_5140	[A gastrointestinal system benign neoplasm that is located_in the gallbladder and derives_from smooth muscle cells.]
vulvar leiomyoma	DOID_5142	[A vulvar benign neoplasm that is located_in smooth muscle cells.]
clear cell variant infiltrating bladder urothelial carcinoma	DOID_6476
large bowel leiomyoma	DOID_5143	[An intestinal benign neoplasm that derives_from smooth muscle cells and that is located_in the large bowel.]
large intestine	UBERON_0000059
childhood teratocarcinoma of the testis	DOID_6474
childhood testicular mixed germ cell tumor	DOID_6161
appendix leiomyoma	DOID_5146	[A gastrointestinal system benign neoplasm that derives_from smooth muscle cells and that is located_in the appendix.]
appendix disease	DOID_60000	[A gastrointestinal system disease that is located_in the appendix.]
dartoic leiomyoma	DOID_5147	[A reproductive organ benign neoplasm that has_material_basis_in the dartos muscle located_in the scrotum or labia majora.]
mitochondrial DNA depletion syndrome 2	DOID_0080120	[A mitochondrial DNA depletion syndrome that is characterized by childhood onset of muscle weakness associated with depletion of mtDNA in skeletal muscle, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the mitochondrial thymidine kinase gene on chromosome 16q21.]
epithelioid neurofibroma	DOID_5149
mitochondrial DNA depletion syndrome 3	DOID_0080121	[A mitochondrial DNA depletion syndrome that is characterized by onset in infancy of progressive liver failure and neurologic abnormalities, hypoglycemia, and increased lactate in body fluids, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the deoxyguanosine kinase gene on chromosome 2p13.]
Hypoglycemia	HP_0001943	[A decreased concentration of glucose in the blood.]
multiple endocrine neoplasia type 4	DOID_0080137
obsolete syphilitic aortitis	DOID_11582
multiple congenital anomalies-hypotonia-seizures syndrome 1	DOID_0080138	[A multiple congenital anomalies-hypotonia-seizures syndrome that is characterized by neonatal hypotonia, lack of psychomotor development, seizures, dysmorphic features, and variable congenital anomalies involving the cardiac, urinary, and gastrointestinal systems and has_material_basis_in homozygous mutation in the PIGN gene on chromosome 18q21.]
phlyctenulosis	DOID_11581
keratoconjunctivitis	DOID_9368