serw-MX  [xml]  
 
    
 DeCS Categories

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.854 Spinal Cord Diseases .
C10.228.854.785 Spinal Cord Vascular Diseases .
C10.500 Nervous System Malformations .
C10.500.680 Neural Tube Defects .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.351 Female Urogenital Diseases .
C13.351.500 Genital Diseases, Female .
C13.351.500.852 Uterine Diseases .
C13.351.500.852.495 Hematometra .
C14 Cardiovascular Diseases .
C14.907 Vascular Diseases .
C14.907.790 Spinal Cord Vascular Diseases .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.666 Nervous System Malformations .
C16.131.666.680 Neural Tube Defects .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.414 Hemorrhage .
C23.550.414.838 Hematoma .
D03 Heterocyclic Compounds .
D03.383 Heterocyclic Compounds, 1-Ring .
D03.383.129 Azoles .
D03.383.129.578 Pyrroles .
D03.383.129.578.840 Tetrapyrroles .
D03.383.129.578.840.500 Porphyrins .
D03.383.129.578.840.500.640 Metalloporphyrins .
D03.383.129.578.840.500.640.587 Heme 4962 .
D03.383.129.578.840.500.640.587.462 Hemin .
D03.633 Heterocyclic Compounds, Fused-Ring .
D03.633.400 Heterocyclic Compounds, 4 or More Rings .
D03.633.400.909 Tetrapyrroles .
D03.633.400.909.500 Porphyrins .
D03.633.400.909.500.640 Metalloporphyrins .
D03.633.400.909.500.640.587 Heme 4962 .
D03.633.400.909.500.640.587.462 Hemin .
D04 Polycyclic Compounds .
D04.345 Macrocyclic Compounds .
D04.345.783 Tetrapyrroles .
D04.345.783.500 Porphyrins .
D04.345.783.500.640 Metalloporphyrins .
D04.345.783.500.640.587 Heme 4962 .
D04.345.783.500.640.587.462 Hemin .
D09 Carbohydrates .
D09.400 Glycoconjugates .
D09.400.410 Glycolipids .
D09.400.410.420 Glycosphingolipids .
D09.400.410.420.025 Acidic Glycosphingolipids .
D09.400.410.420.025.475 Gangliosides .
D09.400.410.420.025.475.510 G(M3) Ganglioside .
D10 Lipids .
D10.390 Glycolipids .
D10.390.470 Glycosphingolipids .
D10.390.470.025 Acidic Glycosphingolipids .
D10.390.470.025.475 Gangliosides .
D10.390.470.025.475.510 G(M3) Ganglioside .
D10.570 Membrane Lipids .
D10.570.877 Sphingolipids .
D10.570.877.360 Glycosphingolipids .
D10.570.877.360.025 Acidic Glycosphingolipids .
D10.570.877.360.025.475 Gangliosides .
D10.570.877.360.025.475.510 G(M3) Ganglioside .
D23 Biological Factors .
D23.767 Pigments, Biological .
D23.767.727 Porphyrins .
D23.767.727.640 Metalloporphyrins .
D23.767.727.640.587 Heme 4962 .
D23.767.727.640.587.462 Hemin .
 
 Terms
 Synonyms & Historicals		Documents
LILACS e MDL		 
Spinal Cord Vascular Diseases .
Vascular Diseases, Spinal Cord .
Hematomyelias .
Hematomyelia .
Posterior Spinal Artery Syndrome .
Pathological processes involving any of the BLOOD VESSELS feeding the SPINAL CORD, such as the anterior and paired posterior spinal arteries or their many branches. Disease processes may include ATHEROSCLEROSIS; EMBOLISM; and ARTERIOVENOUS MALFORMATIONS leading to ISCHEMIA or HEMORRHAGE into the spinal cord (hematomyelia). .
1.00
4120
 
Hematoma .
Hematomas .
A collection of blood outside the BLOOD VESSELS. Hematoma can be localized in an organ, space, or tissue. .
0.73
45119603
 
Hematometra .
Hematometras .
Blood-filled UTERUS. .
0.64
18264
 
Neural Tube Defects .
Acrania .
Developmental Neural Tube Defects .
Iniencephaly .
Neural Tube Developmental Defects .
Neuroenteric Cyst .
Occult Spinal Dysraphism .
Occult Spinal Dysraphism Sequence .
Tethered Spinal Cord Syndrome .
Acranias .
Craniorachischises .
Cyst, Neurenteric .
Cyst, Neuroenteric .
Cysts, Neurenteric .
Cysts, Neuroenteric .
Defect, Neural Tube .
Defects, Neural Tube .
Diastematomyelias .
Dysraphism, Occult Spinal .
Dysraphisms, Occult Spinal .
Exencephalies .
Iniencephalies .
Myelodysplasia, Spinal Cord .
Myelodysplasias, Spinal Cord .
Neural Tube Defect .
Neurenteric Cysts .
Neuroenteric Cysts .
Occult Spinal Dysraphisms .
Spinal Cord Myelodysplasias .
Spinal Dysraphism, Occult .
Spinal Dysraphisms, Occult .
Tethered Cord Syndromes .
Craniorachischisis .
Developmental Defects, Neural Tube .
Diastematomyelia .
Exencephaly .
Neurenteric Cyst .
Spinal Cord Myelodysplasia .
Tethered Cord Syndrome .
Myelodysplasia .
Congenital malformations of the central nervous system and adjacent structures related to defective neural tube closure during the first trimester of pregnancy generally occurring between days 18-29 of gestation. Ectodermal and mesodermal malformations (mainly involving the skull and vertebrae) may occur as a result of defects of neural tube closure. (From Joynt, Clinical Neurology, 1992, Ch55, pp31-41) .
0.62
2507054
 
Hemin .
Alkaline Hematin D-575 .
Chlorohemin .
Ferrihaem .
Ferriheme Chloride .
Ferriprotoporphyrin IX .
Ferriprotoporphyrin IX Chloride .
Panhematin .
Protohemin .
Protohemin IX .
Alkaline Hematin D 575 .
Chloride, Ferriheme .
Chloride, Ferriprotoporphyrin IX .
Hematin D-575, Alkaline .
Ferriprotoporphyrin .
Hematin .
Chloro(7,12-diethenyl-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropanoato(4-)-N(21),N(22),N(23),N(24)) ferrate(2-) dihydrogen. .
0.61
 
G(M3) Ganglioside .
Ganglioside GM3 .
II3NeuAcLacCer .
Sialyl Lactosylceramide .
GM3, Ganglioside .
Lactosylceramide, Sialyl .
Hematoside .
Sialyllactosylceramide .
A ganglioside present in abnormally large amounts in the brain and liver due to a deficient biosynthetic enzyme, G(M3):UDP-N-acetylgalactosaminyltransferase. Deficiency of this enzyme prevents the formation of G(M2) ganglioside from G(M3) ganglioside and is the cause of an anabolic sphingolipidosis. .
0.58
0920