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 DeCS Categories

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.079 Basal Ganglia Diseases .
C10.228.140.079.590 Meige Syndrome .
C10.228.662 Movement Disorders .
C10.228.662.300 Dystonic Disorders .
C10.228.662.300.500 Meige Syndrome .
C14 Cardiovascular Diseases .
C14.280 Heart Diseases .
C14.280.067 Arrhythmias, Cardiac .
C14.280.067.322 Brugada Syndrome .
C14.280.123 Cardiac Conduction System Disease .
C14.280.123.250 Brugada Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.208 Branchio-Oto-Renal Syndrome .
C16.131.260 Chromosome Disorders .
C16.131.260.090 Branchio-Oto-Renal Syndrome .
C16.320 Genetic Diseases, Inborn .
C16.320.100 Brugada Syndrome .
C16.320.180 Chromosome Disorders .
C16.320.180.090 Branchio-Oto-Renal Syndrome .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.745 Lipodystrophy, Congenital Generalized .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.849 Skin Diseases, Metabolic .
C17.800.849.391 Lipodystrophy .
C17.800.849.391.550 Lipodystrophy, Congenital Generalized .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.625 Lipodystrophy .
C18.452.584.625.550 Lipodystrophy, Congenital Generalized .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.745 Lipodystrophy, Congenital Generalized .
C18.452.880 Skin Diseases, Metabolic .
C18.452.880.391 Lipodystrophy .
C18.452.880.391.550 Lipodystrophy, Congenital Generalized .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.288 Disease .
C23.550.288.500 Syndrome .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Meige Syndrome .
Blepharospasm-Oromandibular Dyskinesia .
Blepharospasm-Oromandibular Dystonia Syndrome .
Blepharospasm-Oromandibular Dystonia Syndrome, Idiopathic .
Idiopathic Blepharospasm-Oromandibular Dystonia Syndrome .
Syndrome, Blepharospasm-Oromandibular Dystonia .
Blepharospasm Oromandibular Dyskinesia .
Blepharospasm Oromandibular Dystonia .
Blepharospasm Oromandibular Dystonia Syndrome .
Blepharospasm Oromandibular Dystonia Syndrome, Idiopathic .
Blepharospasm-Oromandibular Dyskinesias .
Blepharospasm-Oromandibular Dystonia Syndromes .
Blepharospasm-Oromandibular Dystonias .
Dyskinesia, Blepharospasm-Oromandibular .
Dyskinesia, Idiopathic Orofacial .
Dyskinesias, Blepharospasm-Oromandibular .
Dyskinesias, Idiopathic Orofacial .
Dystonia Syndrome, Blepharospasm-Oromandibular .
Dystonia Syndromes, Blepharospasm-Oromandibular .
Dystonia, Blepharospasm-Oromandibular .
Dystonias, Blepharospasm-Oromandibular .
Idiopathic Blepharospasm Oromandibular Dystonia Syndrome .
Idiopathic Orofacial Dyskinesias .
Orofacial Dyskinesia, Idiopathic .
Orofacial Dyskinesias, Idiopathic .
Blepharospasm-Oromandibular Dystonia .
Brueghel Syndrome .
Idiopathic Orofacial Dyskinesia .
A syndrome characterized by orofacial DYSTONIA; including BLEPHAROSPASM; forceful jaw opening; lip retraction; platysma muscle spasm; and tongue protrusion. It primarily affects older adults, with an incidence peak in the seventh decade of life. (From Adams et al., Principles of Neurology, 6th ed, p108) .
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Brugada Syndrome .
Brugada ECG Pattern .
Brugada Syndrome 1 .
Brugada Type ECG Pattern .
Right Bundle Branch Block, ST Segment Elevation, and Sudden Death Syndrome .
Sudden Unexplained Death Syndrome .
Sudden Unexplained Nocturnal Death Syndrome .
Sudden Unexplained Nocturnal Death Syndrome (SUNDS) .
Brugada Syndrome 1s .
ECG Pattern, Brugada .
An autosomal dominant defect of cardiac conduction that is characterized by an abnormal ST-segment in leads V1-V3 on the ELECTROCARDIOGRAM resembling a right BUNDLE-BRANCH BLOCK; high risk of VENTRICULAR TACHYCARDIA; or VENTRICULAR FIBRILLATION; SYNCOPAL EPISODE; and possible sudden death. This syndrome is linked to mutations of gene encoding the cardiac SODIUM CHANNEL alpha subunit. .
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Lipodystrophy, Congenital Generalized .
Berardinelli Syndrome .
Berardinelli-Seip Congenital Lipodystrophy .
Berardinelli-Seip Congenital Lipodystrophy Type 1 .
Berardinelli-Seip Congenital Lipodystrophy Type 2 .
Berardinelli-Seip Congenital Lipodystrophy, Type 1 .
Berardinelli-Seip Congenital Lipodystrophy, Type 2 .
Berardinelli-Seip Syndrome .
Brunzell Syndrome .
Brunzell Syndrome (with Bone Cysts) .
Brunzell Syndrome, AGPAT2-Related .
Brunzell Syndrome, BSCL2-Related .
Congenital Generalized Lipodystrophy .
Congenital Generalized Lipodystrophy Type 1 .
Congenital Generalized Lipodystrophy Type 2 .
Congenital Lipoatrophic Diabetes .
Generalized Lipodystrophy .
Lipoatrophic Diabetes, Congenital .
Lipodystrophy, Berardinelli-Seip Congenital, Type 1 .
Lipodystrophy, Berardinelli-Seip Congenital, Type 2 .
Lipodystrophy, Congenital Generalized, Type 1 .
Lipodystrophy, Congenital Generalized, Type 2 .
Lipodystrophy, Total, And Acromegaloid Gigantism .
Seip Syndrome .
Total Lipodystrophy .
Total Lipodystrophy and Acromegaloid Gigantism .
AGPAT2-Related Brunzell Syndrome .
BSCL2-Related Brunzell Syndrome .
Berardinelli Seip Congenital Lipodystrophy .
Berardinelli Seip Congenital Lipodystrophy Type 1 .
Berardinelli Seip Congenital Lipodystrophy Type 2 .
Berardinelli Seip Congenital Lipodystrophy, Type 1 .
Berardinelli Seip Congenital Lipodystrophy, Type 2 .
Berardinelli Seip Syndrome .
Brunzell Syndrome, AGPAT2 Related .
Brunzell Syndrome, BSCL2 Related .
Congenital Generalized Lipodystrophies .
Congenital Lipoatrophic Diabete .
Congenital Lipodystrophy, Berardinelli-Seip .
Diabete, Congenital Lipoatrophic .
Diabetes, Congenital Lipoatrophic .
Generalized Lipodystrophies .
Generalized Lipodystrophies, Congenital .
Generalized Lipodystrophy, Congenital .
Lipoatrophic Diabete, Congenital .
Lipodystrophies, Congenital Generalized .
Lipodystrophies, Generalized .
Lipodystrophies, Total .
Lipodystrophy, Berardinelli-Seip Congenital .
Lipodystrophy, Generalized .
Lipodystrophy, Total .
Syndrome, AGPAT2-Related Brunzell .
Syndrome, BSCL2-Related Brunzell .
Syndrome, Berardinelli .
Syndrome, Berardinelli-Seip .
Syndrome, Brunzell .
Syndrome, Brunzell (with Bone Cysts) .
Syndrome, Seip .
Total Lipodystrophies .
Congenital disorders, usually autosomal recessive, characterized by severe generalized lack of ADIPOSE TISSUE, extreme INSULIN RESISTANCE, and HYPERTRIGLYCERIDEMIA. .
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Syndrome .
Symptom Cluster .
Cluster, Symptom .
Clusters, Symptom .
Symptom Clusters .
Syndromes .
A characteristic symptom complex. .
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Branchio-Oto-Renal Syndrome .
BOF Syndrome .
Branchial Clefts with Characteristic Facies, Growth Retardation, Imperforate Nasolacrimal Duct, and Premature Aging .
Branchio-Otorenal Syndrome .
Branchiooculofacial Syndrome .
Branchiootorenal Dysplasia .
Branchiootorenal Syndrome 1 .
Branchiootorenal Syndrome 2 .
Hemangiomatous Branchial Clefts-Lip Pseudocleft Syndrome .
Lee Root Fenske Syndrome .
Lip Pseudocleft-Hemangiomatous Branchial Cyst Syndrome .
Melnick-Fraser Syndrome .
Branchio Oculo Facial Syndrome .
Branchio Oto Renal Syndrome .
Dysplasia, Branchiootorenal .
Hemangiomatous Branchial Clefts Lip Pseudocleft Syndrome .
Lip Pseudocleft Hemangiomatous Branchial Cyst Syndrome .
Melnick Fraser Syndrome .
Syndrome, BOF .
Syndrome, BOR .
Syndrome, Branchio-Oculo-Facial .
Syndrome, Branchio-Oto-Renal .
Syndrome, Branchiooculofacial .
Syndrome, Melnick-Fraser .
Branchio-Oculo-Facial Syndrome .
Branchio-Otorenal Dysplasia .
BOR Syndrome .
An autosomal dominant disorder manifested by various combinations of preauricular pits, branchial fistulae or cysts, lacrimal duct stenosis, hearing loss, structural defects of the outer, middle, or inner ear, and renal dysplasia. Associated defects include asthenic habitus, long narrow facies, constricted palate, deep overbite, and myopia. Hearing loss may be due to Mondini type cochlear defect and stapes fixation. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed) .
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