All terms in MeSH

Label Id Description
Hybridization, Genetic E05.820.150.390
Breeding E05.820.150
Galactorrhea D005687 [Excessive or inappropriate LACTATION in females or males, and not necessarily related to PREGNANCY. Galactorrhea can occur either unilaterally or bilaterally, and be profuse or sparse. Its most common cause is HYPERPROLACTINEMIA. ]
Sapotaceae D029632 [A plant family of the order Ebenales, subclass Dilleniidae, class Magnoliopsida that are tropical trees which have elongate latex cells. Several members bear sweet edible fruits and produce triterpenoid saponins. , A genus that has triterpenoid saponins in the root. , Argan oil from seeds is consumed raw in the southwest part of Morocco. ]
Galactosamine D005688
Uveitis C11.941.879
Uveal Diseases C11.941
Schisandraceae D029633 [A plant family of the order AUSTROBAILEYALES, class MAGNOLIOPSIDA. ]
Central Nervous System Protozoal Infections C01.610.105.300
Santalaceae D029630 [A plant family of the order Santalales, subclass Rosidae, class Magnoliopsida. They are parasites that form connections (haustoria) to their hosts to obtain water and nutrients. The one-seeded fruit may be surrounded by a brightly colored nut-like structure. ]
Sapindaceae D029631 [A genus of SAPINDACEAE that contains xanthocerasic acid. , The soapberry plant family of the order Sapindales, subclass Rosidae, class Magnoliopsida. Some members contain SAPONINS. ]
Glycogen Storage Disease Type IIb C14.280.238.458
Gagging D005683 [Contraction of the muscle of the PHARYNX caused by stimulation of sensory receptors on the SOFT PALATE, by psychic stimuli, or systemically by drugs. ]
Gait D005684 [Manner or style of walking. ]
Galactans D005685 [Polysaccharides composed of repeating galactose units. They can consist of branched or unbranched chains in any linkages. ]
Galactokinase D005686 [An enzyme that catalyzes reversibly the formation of galactose 1-phosphate and ADP from ATP and D-galactose. Galactosamine can also act as the acceptor. A deficiency of this enzyme results in GALACTOSEMIA. EC 2.7.1.6. ]
Myoclonic Cerebellar Dyssynergia C16.320.400.780.500
Spinocerebellar Degenerations C16.320.400.780
Galactose D005690 [An aldohexose that occurs naturally in the D-form in lactose, cerebrosides, gangliosides, and mucoproteins. Deficiency of galactosyl-1-phosphate uridyltransferase (GALACTOSE-1-PHOSPHATE URIDYL-TRANSFERASE DEFICIENCY DISEASE) causes an error in galactose metabolism called GALACTOSEMIA, resulting in elevations of galactose in the blood. ]
Galactose Dehydrogenases D005691 [D-Galactose:NAD(P)+ 1-oxidoreductases. Catalyzes the oxidation of D-galactose in the presence of NAD+ or NADP+ to D-galactono-gamma-lactone and NADH or NADPH. Includes EC 1.1.1.48 and EC 1.1.1.120. ]