Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
obsolete Papillomaviridae infectious disease	DOID_0050494	[A dsDNA virus infectious disease that results_in infection in animals and humans, has_material_basis_in Papillomaviridae viruses.]
Pseudoterranova	NCBITaxon_6270
Wolffian duct adenoma	DOID_2616	[A reproductive organ benign neoplasm that derives_from glandular epithelial cells and that is located_in the region of the Wolffian duct.]
adrenal gland hyperfunction	DOID_3947
obsolete tertiary syphilitic meningitis	DOID_0050493
Anisakidae	NCBITaxon_6267
susceptibility to mild malaria	OMIM_609148
adrenocortical carcinoma	DOID_3948	[An adrenal cortex cancer that forms in the outer layer of tissue of the adrenal gland and that has_material_basis_in abnormally proliferating cells derives_from epithelial cells.]
obsolete Banna virus encephalitis	DOID_0050496	[A viral infectious disease that results_in inflammation located_in brain, has_material_basis_in Banna virus, which is transmitted_by Culex, and transmitted_by Anopheles mosquitoes. The infection has_symptom fever, and has_symptom headache.]
susceptibility to colorectal cancer 2	OMIM_611469
exanthema subitum	DOID_0050495	[A viral infectious disease that results_in infection in infants and children, located_in skin, has_material_basis_in Human herpesvirus 6 or has_material_basis_in Human herpesvirus 7 and has_symptom sudden high fever, and has_symptom red rash that occurs first on the trunk then spreading to legs and neck.]
obsolete dsDNA virus infectious disease	DOID_0050498	[A DNA virus infectious disease that results_in infection, has_material_basis_in dsDNA viruses, which possess double-stranded DNA.]
obsolete Anelloviridae infectious disease	DOID_0050497	[A ssDNA virus infectious disease that results_in infection in humans, has_material_basis_in Anelloviridae viruses.]
long QT syndrome 2	DOID_0110645	[A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1.]
long QT syndrome 3	DOID_0110646	[A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN5A gene on chromosome 3p22.2.]
long QT syndrome 1	DOID_0110644	[A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4.]
parenchymatous neurosyphilis	DOID_0050490	[A tertiary neurosyphilis that results when chronic meningoencephalitis causes destruction of cortical parenchyma. The infection has_symptom irritability, has_symptom difficulty concentrating, has_symptom deterioration of memory, has_symptom defective judgment, has_symptom headaches, has_symptom insomnia, has_symptom fatigue, and has_symptom lethargy.]
congenital muscular dystrophy due to LMNA mutation	DOID_0110640	[A congenital muscular dystrophy characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the LMNA gene on chromosome 1q22.]
obsolete residual type schizophrenia	DOID_795
obsolete residual schizophrenia in remission	DOID_794