All terms in MeSH

Label Id Description
Neodymium D01.552.550.399.625
Mania D000087122 [A state of elevated excitement with over-activity sometimes accompanied with psychotic symptoms (e.g., PSYCHOMOTOR AGITATION, inflated SELF ESTEEM and flight of ideas). It is often associated with mental disorders (e.g., CYCLOTHYMIC DISORDER; and BIPOLAR DISEASES). ]
COVID-19 Nucleic Acid Testing D000087123 [Diagnosis of COVID-19 by assaying bodily fluids or tissues for the presence of the VIRAL RNA of SARS-COV-2. ]
Burkitt Lymphoma C20.683.515.761.480.150.165
Lymphoma, B-Cell C20.683.515.761.480.150
Dental Records N04.452.859.341
Collagen Type XVIII D12.776.860.300.250.400.537
Sadness F01.470.933
Abuse-Deterrent Formulations E05.916.250.500
Facial Nerve Diseases C10.292.319
Meaningful Use N04.761.744.500
Ranunculaceae B01.650.940.800.575.912.250.836.750
Liver Cirrhosis, Experimental C23.550.355.412.467
Endocarditis, Subacute Bacterial C01.190.249.407
Endocarditis, Bacterial C01.190.249
Deoxyepinephrine D02.092.311.461.200
Kyphoplasty D058498 [Procedures to restore vertebrae to their original shape following vertebral compression fractures by inflating a balloon inserted into the vertebrae, followed by removal of the balloon and injection of BONE CEMENTS to fill the cavity. ]
Retinal Dystrophies D058499 [A group of disorders involving predominantly the posterior portion of the ocular fundus, due to degeneration in the sensory layer of the RETINA; RETINAL PIGMENT EPITHELIUM; BRUCH MEMBRANE; CHOROID; or a combination of these tissues. ]
Arsenates D01.075.025
Walker-Warburg Syndrome D058494 [Rare autosomal recessive lissencephaly type 2 associated with congenital MUSCULAR DYSTROPHY and eye anomalies (e.g., RETINAL DETACHMENT; CATARACT; MICROPHTHALMOS). It is often associated with additional brain malformations such as HYDROCEPHALY and cerebellar hypoplasia and is the most severe form of the group of related syndromes (alpha-dystroglycanopathies) with common congenital abnormalities in the brain, eye and muscle development. ]