Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
type 2 papillary adenoma of the kidney	DOID_6259
nephrotic syndrome type 11	DOID_0080385	[A familial nephrotic syndrome characterized by onset in the first decade of life of steroid resistant progressive renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the NUP107 gene on chromosome 12q15.]
nephrotic syndrome type 5	DOID_0080380	[A familial nephrotic syndrome characterized by prenatal or neonatal onset of progressive renal failure with proteinurea and edema that has_material_basis_in homozygous or compound heterozygous mutation in the LAMB2 gene on chromosome 3p.]
nephrotic syndrome type 13	DOID_0080381	[A familial nephrotic syndrome characterized by early onset of steroid-resistant nephrotic syndrome and focal segmental glomerulosclerosis that has_material_basis_in homozygous mutation in the NUP205 gene on chromosome 7q33.]
patellar tendinitis	DOID_10471
tendinitis	DOID_971
motor paralysis	SYMP_0000848	[Motor paralysis is a paralysis where there is a complete or partial loss of function the voluntary muscles.]
obsolete candidal pneumonia	DOID_10472	[A candidiasis that involves inflammation of the lung caused by Candida species either by hematogenous dissemination or by bronchial extension in patients with oropharyngeal candidiasis. The symptoms include fever, tachypnea, dyspnea, and chest pain.]
stillbirth	SYMP_0000849	[Stillbirth is a reproductive system symptom characterized by the birth of a dead fetus, occurs when a fetus which has died in the uterus or during labor or delivery exits a woman's body.]
chest hyperemia	SYMP_0000846	[Hyperemia of the chest is a cardiovascular system symptom consisting of an excess of blood in the tissues of the chest as from an increased flow of blood due to vasodilation.]
spastic paralysis	SYMP_0000847	[Spastic paralysis is a paralysis characterized by tonic spasm of the affected muscles and with increased tendon reflexes.]
face hyperemia	SYMP_0000844	[Hyperemia of the face is a head symptom consisting of an excess of blood in the tissues of the face as from an increased flow of blood due to vasodilation.]
orofacial cleft 3	DOID_0080397	[An orofacial cleft that has_material_basis_in variation in the chromosomal region 19q13.]
orofacial cleft	DOID_0050567	[A physical disorder that is characterized by cleft lip and/or cleft palate that result in feeding, speech and hearing problems caused by failures during development.]
hyperemia of the neck	SYMP_0000845	[Hyperemia of the neck is a neck symptom consisting of an excess of blood in the tissues of the neck as from an increased flow of blood due to vasodilation.]
orofacial cleft 4	DOID_0080398	[An orofacial cleft that has_material_basis_in variation in the 4q21-q31 chromosomal region.]
active hyperemia	SYMP_0000842	[Active hyperemia is a hyperemia occuring due to the dilation of arteriolar smooth muscle to increase blood flow in response to an increase in metabolism.]
orofacial cleft 5	DOID_0080399	[An orofacial cleft that has_material_basis_in mutation in the MSX1 gene on chromosome 4p16.]
functional hyperemia	SYMP_0000843	[Functional hyperemia is a hyperemia occuring due to an increase in blood flow to a tissue due to the presence of metabolites and a change in general conditions.]
gastric cardia carcinoma	DOID_6270