serw-MX  [xml]  

 DeCS Categories

B01 Eukaryota .
B01.050 Animals .
B01.050.150 Chordata .
B01.050.150.900 Vertebrates .
B01.050.150.900.493 Fishes .
B01.050.150.900.493.370 Elasmobranchii .
B01.050.150.900.493.370.853 Sharks .
C10 Nervous System Diseases .
C10.900 Trauma, Nervous System .
C10.900.300 Craniocerebral Trauma .
C10.900.300.087 Brain Injuries .
C10.900.300.087.850 Shaken Baby Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.860 Smith-Lemli-Opitz Syndrome .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.850 Smith-Lemli-Opitz Syndrome .
C16.320.565.925 Steroid Metabolism, Inborn Errors .
C16.320.565.925.875 Smith-Lemli-Opitz Syndrome .
C17 Skin and Connective Tissue Diseases .
C17.300 Connective Tissue Diseases .
C17.300.540 Mixed Connective Tissue Disease .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.500 Dyslipidemias .
C18.452.584.500.937 Smith-Lemli-Opitz Syndrome .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.850 Smith-Lemli-Opitz Syndrome .
C18.452.648.925 Steroid Metabolism, Inborn Errors .
C18.452.648.925.875 Smith-Lemli-Opitz Syndrome .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.288 Disease .
C23.550.288.500 Syndrome .
C26 Wounds and Injuries .
C26.915 Trauma, Nervous System .
C26.915.300 Craniocerebral Trauma .
C26.915.300.200 Brain Injuries .
C26.915.300.200.825 Shaken Baby Syndrome .
SH1 Health Sciences, Technology and Innovation Management .
SH1.010 Policies and Cooperation in Science, Technology and Innovation .
SH1.010.020 International Cooperation .
SH1.010.020.060 Science and Technology Information Networks .
SH1. Scientists for Health and Research for Development .
 Synonyms & Historicals
Mixed Connective Tissue Disease .
MCTD 6868 .
Syndrome, Sharp .
Connective Tissue Disease, Mixed .
Sharp Syndrome .
A syndrome with overlapping clinical features of systemic lupus erythematosus, scleroderma, polymyositis, and Raynaud's phenomenon. The disease is differentially characterized by high serum titers of antibodies to ribonuclease-sensitive extractable (saline soluble) nuclear antigen and a "speckled" epidermal nuclear staining pattern on direct immunofluorescence. .
Syndrome .
Symptom Cluster .
Cluster, Symptom .
Clusters, Symptom .
Symptom Clusters .
Syndromes .
A characteristic symptom complex. .
Shaken Baby Syndrome .
Brain injuries resulted from vigorous shaking of an infant or young child held by the chest, shoulders, or extremities causing extreme cranial acceleration. It is characterized by the intracranial and intraocular hemorrhages with no evident external trauma. Serious cases may result in death. .
Sharks .
Shark .
A group of elongate elasmobranchs. Sharks are mostly marine fish, with certain species large and voracious. .
Smith-Lemli-Opitz Syndrome .
7-Dehydrocholesterol Reductase Deficiency .
Hyperotosis Corticalis Generalisata Familiaris .
Lethal Acrodysgenital Syndrome .
Polydactyly, Sex Reversal, Renal Hypoplasia, And Unilobar Lung .
RSH Syndrome .
RSH-SLO Syndrome .
Rutledge Friedman Harrod Syndrome .
Rutledge Lethal Multiple Congenital Anomaly Syndrome .
SLO Syndrome .
Smith Lemli Opitz syndrome, type 1 .
Smith-Lemli-Opitz Syndrome, Type 1 .
Smith-Lemli-Opitz Syndrome, Type 2 .
Smith-Lemli-Opitz Syndrome, Type I .
Smith-Lemli-Opitz Syndrome, Type II .
7-Dehydrocholesterol Reductase Deficiencies .
Acrodysgenital Syndrome, Lethal .
Acrodysgenital Syndromes, Lethal .
Deficiencies, 7-Dehydrocholesterol Reductase .
Deficiency, 7-Dehydrocholesterol Reductase .
Lethal Acrodysgenital Syndromes .
RSH SLO Syndrome .
RSH Syndromes .
RSH-SLO Syndromes .
Reductase Deficiencies, 7-Dehydrocholesterol .
Reductase Deficiency, 7-Dehydrocholesterol .
SLO Syndromes .
Smith Lemli Opitz Syndrome .
Smith Lemli Opitz Syndrome, Type 2 .
Smith Lemli Opitz Syndrome, Type I .
Smith Lemli Opitz Syndrome, Type II .
Syndrome, Lethal Acrodysgenital .
Syndrome, RSH .
Syndrome, SLO .
Syndromes, RSH .
Syndromes, SLO .
An autosomal recessive disorder of CHOLESTEROL metabolism. It is caused by a deficiency of 7-dehydrocholesterol reductase, the enzyme that converts 7-dehydrocholesterol to cholesterol, leading to an abnormally low plasma cholesterol. This syndrome is characterized by multiple CONGENITAL ABNORMALITIES, growth deficiency, and INTELLECTUAL DISABILITY. .
Scientists for Health and Research for Development .
Digital network based on validated information on ongoing medical and health related research, researchers and institutions. ( ( .