serw-MX  [xml]  
 


    
 DeCS Categories

B01 Eukaryota .
B01.650 Plants .
B01.650.940 Viridiplantae .
B01.650.940.800 Streptophyta .
B01.650.940.800.575 Embryophyta .
B01.650.940.800.575.912 Tracheophyta .
B01.650.940.800.575.912.250 Magnoliopsida .
B01.650.940.800.575.912.250.198 Caryophyllanae .
B01.650.940.800.575.912.250.198.500 Caryophyllales .
B01.650.940.800.575.912.250.198.500.250 Caryophyllaceae .
B01.650.940.800.575.912.250.198.500.250.655 Silene .
B01.650.940.800.575.912.250.859 Rosanae .
B01.650.940.800.575.912.250.859.500 Celastrales .
B01.650.940.800.575.912.250.859.500.750 Celastraceae .
B01.650.940.800.575.912.250.859.500.750.155 Catha .
C05 Musculoskeletal Diseases .
C05.660 Musculoskeletal Abnormalities .
C05.660.207 Craniofacial Abnormalities .
C05.660.207.103 22q11 Deletion Syndrome .
C05.660.207.103.500 DiGeorge Syndrome .
C14 Cardiovascular Diseases .
C14.240 Cardiovascular Abnormalities .
C14.240.400 Heart Defects, Congenital .
C14.240.400.021 22q11 Deletion Syndrome .
C14.240.400.021.500 DiGeorge Syndrome .
C14.280 Heart Diseases .
C14.280.400 Heart Defects, Congenital .
C14.280.400.044 22q11 Deletion Syndrome .
C14.280.400.044.500 DiGeorge Syndrome .
C15 Hemic and Lymphatic Diseases .
C15.604 Lymphatic Diseases .
C15.604.451 Lymphatic Abnormalities .
C15.604.451.249 22q11 Deletion Syndrome .
C15.604.451.249.500 DiGeorge Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.019 22q11 Deletion Syndrome .
C16.131.077.019.500 DiGeorge Syndrome .
C16.131.240 Cardiovascular Abnormalities .
C16.131.240.400 Heart Defects, Congenital .
C16.131.240.400.021 22q11 Deletion Syndrome .
C16.131.240.400.021.500 DiGeorge Syndrome .
C16.131.260 Chromosome Disorders .
C16.131.260.019 22q11 Deletion Syndrome .
C16.131.260.019.500 DiGeorge Syndrome .
C16.131.482 Lymphatic Abnormalities .
C16.131.482.249 22q11 Deletion Syndrome .
C16.131.482.249.500 DiGeorge Syndrome .
C16.131.621 Musculoskeletal Abnormalities .
C16.131.621.207 Craniofacial Abnormalities .
C16.131.621.207.103 22q11 Deletion Syndrome .
C16.131.621.207.103.500 DiGeorge Syndrome .
C16.320 Genetic Diseases, Inborn .
C16.320.180 Chromosome Disorders .
C16.320.180.019 22q11 Deletion Syndrome .
C16.320.180.019.500 DiGeorge Syndrome .
C19 Endocrine System Diseases .
C19.642 Parathyroid Diseases .
C19.642.482 Hypoparathyroidism .
C19.642.482.500 22q11 Deletion Syndrome .
C19.642.482.500.500 DiGeorge Syndrome .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.612 Pain 7776 .
C23.888.592.612.233 Chest Pain .
D09 Carbohydrates .
D09.698 Polysaccharides .
D09.698.629 Oligosaccharides .
D09.698.629.802 Trisaccharides .
D09.698.629.802.100 Acarbose .
HP4 Materia Medica .
HP4.018 Homeopathic Remedy .
HP4.018.313 Homeopathic Remedy G .
HP4.018.313.113 Galium aparine .
SP4 Environmental Health .
SP4.016 Water Resources .
SP4.016.132 Water .
SP4.016.132.553 Surface Waters .
SP4.016.132.553.894 Basins .
SP8 Disasters .
SP8.473 Risk 17142 .
SP8.473.654 Hazards .
SP8.473.654.482 Geography .
SP8.473.654.482.087 Basins .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Chest Pain .
Precordial Catch .
Precordial Catch Syndrome .
Texidor's Twinge .
Chest Pains .
Pain, Chest .
Pains, Chest .
Syndrome, Precordial Catch .
Texidor Twinge .
Pressure, burning, or numbness in the chest. .
1.00
 
Basins .
Catchment .
All land within the confines of a drainage divide. All surface water having a common outlet (Material II - IDNDR, 1992). A topographic or structural low area that generally receives thicker deposits of sediments than adjacent areas; the low areas tend to sink more readily, partly because of the weight of the thicker sediments; the term also denotes an area of relatively deep water adjacent to shallow-water shelf areas. (Illinois State Geological Survey - ISGS Glossary of Geologic Terms - http://www.isgs.uiuc.edu/tours/outliers/glossary.htm) .
0.49
 
DiGeorge Syndrome .
22q11.2 Deletion Syndrome .
22q11.2DS .
Autosomal Dominant Opitz G-Bbb Syndrome .
Catch22 .
Conotruncal Anomaly Face Syndrome .
Conotruncal Anomaly Face Syndrome (CTAF) .
Deletion 22q11.2 Syndrome .
DiGeorge Anomaly .
DiGeorge Sequence .
Familial Third and Fourth Pharyngeal Pouch Syndrome .
Hypoplasia of Thymus and Parathyroids .
Pharyngeal Pouch Syndrome .
Sedlackova Syndrome .
Shprintzen Syndrome .
Shprintzen VCF Syndrome .
Third and Fourth Pharyngeal Pouch Syndrome .
Thymic Aplasia Syndrome .
VCF Syndrome .
Velo-Cardio-Facial Syndrome .
Autosomal Dominant Opitz G Bbb Syndrome .
Deletion Syndrome, 22q11.2 .
Syndrome, DiGeorge .
Syndrome, Sedlackova .
Syndrome, Shprintzen .
Syndrome, VCF .
Syndrome, Velo-Cardio-Facial .
Syndrome, Velocardiofacial .
Velo Cardio Facial Syndrome .
Velocardiofacial Syndrome .
Congenital syndrome characterized by a wide spectrum of characteristics including the absence of the THYMUS and PARATHYROID GLANDS resulting in T-cell immunodeficiency, HYPOCALCEMIA, defects in the outflow tract of the heart, and craniofacial anomalies. .
0.48
 
Acarbose .
Bay g 5421 .
Glucobay .
Glucor .
Glumida .
Prandase .
Precose .
An inhibitor of ALPHA-GLUCOSIDASES that retards the digestion and absorption of DIETARY CARBOHYDRATES in the SMALL INTESTINE. .
0.46
 
Galium aparine .
Clivers .
Stickywilly .
Stickyweed .
Stickyleaf .
Catchweed .
Robin-Run-the-Hedge .
Coachweed .
Homeopathic remedy. Abbrev.: "gali.". .
0.46
 
Silene .
Catchflies, Pink .
Pink Catchflies .
Pink Catchfly .
Silenes .
Catchfly, Pink .
Campion .
A plant genus of the family CARYOPHYLLACEAE. The common name of campion is also used with LYCHNIS. The common name of 'pink' can be confused with other plants. .
0.42
 
Catha .
Catha edulis .
Mairungi .
Miraa .
Qat Plant .
Catha eduli .
Cathas .
Khats .
Mairungus .
Miraas .
Plant, Qat .
Plants, Qat .
Qat Plants .
edulis, Catha .
Khat 23483 .
A plant genus of the family CELASTRACEAE. The leafy stems of khat are chewed by some individuals for stimulating effect. Members contain ((+)-norpseudoephedrine), cathionine, cathedulin, cathinine & cathidine. .
0.40