All terms in MeSH

Label Id Description
Hyperostosis, Cortical, Congenital D006958 [A disease of young infants characterized by soft tissue swellings over the affected bones, fever, and irritability, and marked by periods of remission and exacerbation. (Dorland, 27th ed) ]
Laryngismus C08.360.895.500
Hyperoxaluria D006959 [Excretion of an excessive amount of OXALATES in the urine. ]
Maternal Exposure N06.850.460.350.145
Hyperlipoproteinemia Type III D006952 [An autosomal recessively inherited disorder characterized by the accumulation of intermediate-density lipoprotein (IDL or broad-beta-lipoprotein). IDL has a CHOLESTEROL to TRIGLYCERIDES ratio greater than that of VERY-LOW-DENSITY LIPOPROTEINS. This disorder is due to mutation of APOLIPOPROTEINS E, a receptor-binding component of VLDL and CHYLOMICRONS, resulting in their reduced clearance and high plasma levels of both cholesterol and triglycerides. ]
Patient Compliance F01.100.150.750.500.600
Hyperlipoproteinemia Type IV D006953 [A hypertriglyceridemia disorder, often with autosomal dominant inheritance. It is characterized by the persistent elevations of plasma TRIGLYCERIDES, endogenously synthesized and contained predominantly in VERY-LOW-DENSITY LIPOPROTEINS (pre-beta lipoproteins). In contrast, the plasma CHOLESTEROL and PHOSPHOLIPIDS usually remain within normal limits. ]
Ophthalmoplegia, Chronic Progressive External C18.452.660.560.700
Hyperlipoproteinemia Type V D006954 [A severe type of hyperlipidemia, sometimes familial, that is characterized by the elevation of both plasma CHYLOMICRONS and TRIGLYCERIDES contained in VERY-LOW-DENSITY LIPOPROTEINS. Type V hyperlipoproteinemia is often associated with DIABETES MELLITUS and is not caused by reduced LIPOPROTEIN LIPASE activity as in HYPERLIPOPROTEINEMIA TYPE I . ]
Hypernatremia D006955 [Excessive amount of sodium in the blood. (Dorland, 27th ed) ]
Hyperlipidemia, Familial Combined D006950 [A type of familial lipid metabolism disorder characterized by a variable pattern of elevated plasma CHOLESTEROL and/or TRIGLYCERIDES. Multiple genes on different chromosomes may be involved, such as the major late transcription factor (UPSTREAM STIMULATORY FACTORS) on CHROMOSOME 1. ]
Hyperlipoproteinemias D006951 [Conditions with abnormally elevated levels of LIPOPROTEINS in the blood. They may be inherited, acquired, primary, or secondary. Hyperlipoproteinemias are classified according to the pattern of lipoproteins on electrophoresis or ultracentrifugation. ]
Tuberculosis, Laryngeal C08.730.860
Root Canal Preparation E06.397.778.889
Whole Grains G07.203.300.300.550.500
Edible Grain G07.203.300.300.550
Pleural Effusion, Malignant C08.528.694.700
Divorce I01.880.853.150.423.500.300
Marital Status I01.880.853.150.423.500
Apoptotic Protease-Activating Factor 1 D12.776.476.075.358.124