Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
bladder lateral wall cancer	DOID_11593
urinary bladder cancer	DOID_11054	[An urinary system cancer that results_in malignant growth located_in the urinary bladder.]
obsolete Mumps virus hepatitis	DOID_10263	[A Mumps virus infectious disease that results_in inflammation located_in liver, has_material_basis_in Mumps virus, which is transmitted_by contact with the oronasal secretions of an infected person. The infection causes swelling of parotid gland and has_symptom fever, has_symptom nausea, has_symptom anorexia, and has_symptom dark urine.]
Palpitations	HP_0001962	[A sensation that the heart is pounding or racing, which is a non-specific sign but may be a manifestation of arrhythmia.]
Arrhythmia	HP_0011675	[Any cardiac rhythm other than the normal sinus rhythm. Such a rhythm may be either of sinus or ectopic origin and either regular or irregular. An arrhythmia may be due to a disturbance in impulse formation or conduction or both.]
microcephaly and chorioretinopathy 1	DOID_0080105	[A syndrome that is characterized by delayed psychomotor development and visual impairment, often accompanied by short stature and has_material_basis_in homozygous or compound heterozygous mutation in the TUBGCP6 gene.]
microcephaly and chorioretinopathy 2	DOID_0080106	[A syndrome that is characterized by delayed psychomotor development, visual impairment, and short stature and has_material_basis_in homozygous mutation in the PLK4 gene.]
discharging ear	DOID_10261
auditory system disease	DOID_2742	[A sensory system disease that is characterized by auditory dysfunction located_in the auditory system.]
microcephaly and chorioretinopathy 3	DOID_0080107	[A syndrome that is characterized by congenital microcephaly and chorioretinal dysplasia associated with poor vision and nystagmus and has_material_basis_in compound heterozygous mutation in the TUBGCP4 gene.]
congenital myopathy	DOID_0080100
myopathy	DOID_423	[A muscular disease in which the muscle fibers do not function resulting in muscular weakness.]
Compton-North congenital myopathy	DOID_0080101
congenital fiber-type disproportion	DOID_0080102
cylindrical spirals myopathy	DOID_0080103
Frey syndrome	DOID_11599
subendocardial infarction acute myocardial infarction	DOID_10266
acute myocardial infarction	DOID_9408
myoglobinuria	DOID_0080108	[A myopathy that is characterized by an increased urinary excretion of myoglobin.]
obsolete cold injury syndrome of newborn	DOID_11597