|
Desipramine
|
D03.633.300.240.281 |
|
|
Cordyline
|
D031406 |
[A plant genus of the family Asparagaceae that contains spirostanol & furostanol SAPONINS.
] |
|
Crinum
|
D031407 |
[A plant genus of the family Amaryllidaceae that contains ALKALOIDS.
] |
|
Curculigo
|
D031408 |
[A plant genus of the family Hypoxidaceae that contains curculin and cycloartane saponins.
] |
|
Etanercept
|
D000068800 |
[A recombinant version of soluble human TNF receptor fused to an IgG FC fragment that binds specifically to TUMOR NECROSIS FACTOR and inhibits its binding with endogenous TNF receptors. It prevents the inflammatory effect of TNF and is used to treat RHEUMATOID ARTHRITIS; PSORIATIC ARTHRITIS and ANKYLOSING SPONDYLITIS.
] |
|
Dracaena
|
D031409 |
[A plant genus of the family Asparagaceae. The common name of "dragon's blood" is also used for CROTON and Daemonorops (ARECACEAE).
] |
|
Adapalene, Benzoyl Peroxide Drug Combination
|
D000068801 |
[A pharmaceutical preparation of adapalene and benzoyl peroxide that is used as a DERMATOLOGIC AGENT for the topical treatment of ACNE.
] |
|
Hemoglobin E
|
D006446 |
[An abnormal hemoglobin that results from the substitution of lysine for glutamic acid at position 26 of the beta chain. It is most frequently observed in southeast Asian populations.
] |
|
Osteochondromatosis
|
C05.116.099.708.670.615 |
|
|
Hemoglobin H
|
D006447 |
[An abnormal hemoglobin composed of four beta chains. It is caused by the reduced synthesis of the alpha chain. This abnormality results in ALPHA-THALASSEMIA.
] |
|
Hemoglobin J
|
D006448 |
[A group of abnormal hemoglobins with similar electrophoretic characteristics. They have faster electrophoretic mobility and different amino acid substitutions in either the alpha or beta chains than normal adult hemoglobin. Some of the variants produce hematologic abnormalities, others result in no clinical disorders.
] |
|
Hemoglobin M
|
D006449 |
[A group of abnormal hemoglobins in which amino acid substitutions take place in either the alpha or beta chains but near the heme iron. This results in facilitated oxidation of the hemoglobin to yield excess methemoglobin which leads to cyanosis.
] |
|
Glycated Hemoglobin A
|
D006442 |
[Products of non-enzymatic reactions between GLUCOSE and HEMOGLOBIN A, occurring as a minor fraction of the hemoglobin components of human erythrocytes. Hemoglobin A1c is hemoglobin A with glucose covalently bound to the terminal VALINE of the beta chain. Glycated hemoglobin A is used as an index of the average blood sugar level over a lifetime of erythrocytes.
] |
|
Levorphanol
|
D03.132.577.249.463 |
|
|
Hemoglobin A2
|
D006443 |
[An adult hemoglobin component normally present in hemolysates from human erythrocytes in concentrations of about 3%. The hemoglobin is composed of two alpha chains and two delta chains. The percentage of HbA2 varies in some hematologic disorders, but is about double in beta-thalassemia.
] |
|
Sporozoites
|
B05.775.740.600.800 |
|
|
Oocysts
|
B05.775.740.600 |
|
|
Hemoglobin C
|
D006444 |
[A commonly occurring abnormal hemoglobin in which lysine replaces a glutamic acid residue at the sixth position of the beta chains. It results in reduced plasticity of erythrocytes.
] |
|
Hemoglobin C Disease
|
D006445 |
[A disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal discomfort, splenomegaly, and slight jaundice.
] |
|
Hemoglobin SC Disease
|
D006450 |
[One of the sickle cell disorders characterized by the presence of both hemoglobin S and hemoglobin C. It is similar to, but less severe than sickle cell anemia.
] |
