|
Setariasis
|
C01.610.701.377.820 |
|
|
Glycerol-3-Phosphate O-Acyltransferase
|
D005992 |
[An enzyme that transfers acyl groups from acyl-CoA to glycerol-3-phosphate to form monoglyceride phosphates. It acts only with CoA derivatives of fatty acids of chain length above C-10. Also forms diglyceride phosphates. EC 2.3.1.15.
] |
|
Swertia
|
D029967 |
[A plant genus of the family GENTIANACEAE. It is a source of swertiapuniside and IRIDOID GLYCOSIDES.
] |
|
Glycerolphosphate Dehydrogenase
|
D005993 |
|
|
Fagus
|
D029964 |
[A plant genus of the family FAGACEAE.
] |
|
Glycerophosphates
|
D005994 |
[Any salt or ester of glycerophosphoric acid.
] |
|
Gentianaceae
|
D029965 |
[A plant genus of the family GENTIANACEAE that is used medicinally in India. Its common name of shankhpushpi is also used for EVOLVULUS alsinoides.
, A plant family of the order Gentianales, subclass Asteridae, class Magnoliopsida.
] |
|
Fructose Metabolism, Inborn Errors
|
D015318 |
[Inherited abnormalities of fructose metabolism, which include three known autosomal recessive types: hepatic fructokinase deficiency (essential fructosuria), hereditary fructose intolerance, and hereditary fructose-1,6-diphosphatase deficiency. Essential fructosuria is a benign asymptomatic metabolic disorder caused by deficiency in fructokinase, leading to decreased conversion of fructose to fructose-1-phosphate and alimentary hyperfructosemia, but with no clinical dysfunction; may produce a false-positive diabetes test.
] |
|
Genetic Counseling
|
H01.158.273.343.385.500.384 |
|
|
Fructose-1,6-Diphosphatase Deficiency
|
D015319 |
[An autosomal recessive fructose metabolism disorder due to absent or deficient fructose-1,6-diphosphatase activity. Gluconeogenesis is impaired, resulting in accumulation of gluconeogenic precursors (e.g., amino acids, lactate, ketones) and manifested as hypoglycemia, ketosis, and lactic acidosis. Episodes in the newborn infant are often lethal. Later episodes are often brought on by fasting and febrile infections. As patients age through early childhood, tolerance to fasting improves and development becomes normal.
] |
|
Proto-Oncogene Proteins c-bcl-2
|
D12.776.476.075.718 |
|
|
Genetic Therapy
|
D015316 |
[The processes by which highly specific gene sequences in a host cell are targeted and regulated for the purpose of reversing and or curing a disease.
, Techniques and strategies which include the use of coding sequences and other conventional or radical means to transform or modify cells for the purpose of treating or reversing disease conditions.
] |
|
Biogenic Polyamines
|
D015317 |
[Biogenic amines having more than one amine group. These are long-chain aliphatic compounds that contain multiple amino and/or imino groups. Because of the linear arrangement of positive charge on these molecules, polyamines bind electrostatically to ribosomes, DNA, and RNA.
] |
|
Hand Deformities, Congenital
|
C16.131.621.585.988.500 |
|
|
Angelica archangelica
|
D029970 |
[A plant species of the family Apiaceae that contains COUMARINS.
] |
|
Cefotiam
|
D015310 |
[One of the CEPHALOSPORINS that has a broad spectrum of activity against both gram-positive and gram-negative microorganisms.
] |
|
Cefmetazole
|
D015311 |
[A semisynthetic cephamycin antibiotic with a broad spectrum of activity against both gram-positive and gram-negative microorganisms. It has a high rate of efficacy in many types of infection and to date no severe side effects have been noted.
] |
|
Crepis
|
B01.650.940.800.575.912.250.100.255 |
|
|
Child Psychiatry
|
F04.096.544.193 |
|
|
Chemoradiotherapy, Adjuvant
|
E02.815.160.500 |
|
