All terms in MeSH

Label Id Description
Luminescent Measurements E05.196.712.516
Lysinoalanine D12.125.042.475
Amniocentesis E04.665.600.309
Guillain-Barre Syndrome C10.314.750.450
Golgi-Mazzoni Corpuscles A08.800.950.750.300
Bland White Garland Syndrome C14.280.400.210.249
Disability Studies I02.158.405.500
Interdisciplinary Studies I02.158.405
Valsartan D12.125.070.950.550
Thapsigargin D02.455.426.392.368.284.500.888
Sesquiterpenes, Guaiane D02.455.426.392.368.284.500
Laminopathies D000083083 [Congenital neuromuscular and muscular dystrophy diseases associated with mutations in the LAMIN TYPE A (Lamin A/C or LMNA gene). It includes CARDIOMYOPATHY, DILATED, 1A; CHARCOT-MARIE-TOOTH DISEASE, type 2B1; EMERY-DREIFUSS MUSCULAR DYSTROPHY, types 2 and 3; HUTCHINSON-GILFORD PROGERIA SYNDROME; LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2; Malouf syndrome; Mandibuloacral dysplasia; LMNA-related muscular dystrophy; Restrictive dermopathy, lethal; Heart-hand syndrome, Slovenian type. ]
Water Resources J01.728.500
Natural Resources J01.728
Collagen Type XII D12.776.860.300.250.400.550.300
Trigeminal Neuralgia C10.292.319.625.700.700
Popliteal Artery Entrapment Syndrome D000083082 [Entrapment of the POPLITEAL ARTERY in the LEG due to an abnormal course of the artery often associated with onset of development and/or overuse of the gastrocnemius or popliteus muscles on the back of the leg. It is most often associated with runners and other athletes with enlarged calf muscle that compresses the popliteal artery. ]
NG-Nitroarginine Methyl Ester D12.125.068.050.525
Enterovirus, Bovine B04.820.578.750.284.200
Superoxides D01.650.550.750.800