serw-MX  [xml]  
 


    
 Categorias DeCS

C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.725 Osteoarthropathy, Primary Hypertrophic .
C05.550 Joint Diseases .
C05.550.648 Osteoarthropathy, Primary Hypertrophic .
C08 Respiratory Tract Diseases .
C08.127 Bronchial Diseases .
C08.127.384 Bronchiectasis .
C08.127.384.500 Kartagener Syndrome .
C08.200 Ciliary Motility Disorders .
C08.200.531 Kartagener Syndrome .
C08.695 Respiratory System Abnormalities .
C08.695.501 Kartagener Syndrome .
C09 Otorhinolaryngologic Diseases .
C09.150 Ciliary Motility Disorders .
C09.150.531 Kartagener Syndrome .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.079 Basal Ganglia Diseases .
C10.228.140.079.898 Tourette Syndrome .
C10.228.662 Movement Disorders .
C10.228.662.825 Tic Disorders .
C10.228.662.825.800 Tourette Syndrome .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.850 Tourette Syndrome .
C14 Cardiovascular Diseases .
C14.240 Cardiovascular Abnormalities .
C14.240.400 Heart Defects, Congenital .
C14.240.400.280 Dextrocardia .
C14.240.400.280.500 Kartagener Syndrome .
C14.280 Heart Diseases .
C14.280.400 Heart Defects, Congenital .
C14.280.400.280 Dextrocardia .
C14.280.400.280.500 Kartagener Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.245 Ciliopathies .
C16.131.077.245.500 Ciliary Motility Disorders .
C16.131.077.245.500.531 Kartagener Syndrome .
C16.131.077.350 Ectodermal Dysplasia .
C16.131.077.350.198 Ectodermal Dysplasia 1, Anhidrotic .
C16.131.077.445 Incontinentia Pigmenti .
C16.131.240 Cardiovascular Abnormalities .
C16.131.240.400 Heart Defects, Congenital .
C16.131.240.400.280 Dextrocardia .
C16.131.240.400.280.500 Kartagener Syndrome .
C16.131.740 Respiratory System Abnormalities .
C16.131.740.501 Kartagener Syndrome .
C16.131.810 Situs Inversus .
C16.131.810.250 Dextrocardia .
C16.131.810.250.500 Kartagener Syndrome .
C16.131.831 Skin Abnormalities .
C16.131.831.350 Ectodermal Dysplasia .
C16.131.831.350.198 Ectodermal Dysplasia 1, Anhidrotic .
C16.131.831.580 Incontinentia Pigmenti .
C16.320 Genetic Diseases, Inborn .
C16.320.184 Ciliopathies .
C16.320.184.500 Ciliary Motility Disorders .
C16.320.184.500.531 Kartagener Syndrome .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.116 Ectodermal Dysplasia 1, Anhidrotic .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.820 Tourette Syndrome .
C16.320.480 Kartagener Syndrome .
C16.320.718 Osteoarthropathy, Primary Hypertrophic .
C16.320.850 Skin Diseases, Genetic .
C16.320.850.250 Ectodermal Dysplasia .
C16.320.850.250.198 Ectodermal Dysplasia 1, Anhidrotic .
C16.320.850.420 Incontinentia Pigmenti .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.621 Pigmentation Disorders .
C17.800.621.497 Incontinentia Pigmenti .
C17.800.804 Skin Abnormalities .
C17.800.804.350 Ectodermal Dysplasia .
C17.800.804.350.198 Ectodermal Dysplasia 1, Anhidrotic .
C17.800.804.580 Incontinentia Pigmenti .
C17.800.827 Skin Diseases, Genetic .
C17.800.827.250 Ectodermal Dysplasia .
C17.800.827.250.198 Ectodermal Dysplasia 1, Anhidrotic .
C17.800.827.420 Incontinentia Pigmenti .
F03 Mental Disorders .
F03.625 Neurodevelopmental Disorders .
F03.625.992 Tic Disorders .
F03.625.992.850 Tourette Syndrome .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Ectodermal Dysplasia 1, Anhidrotic .
Anhidrotic Ectodermal Dysplasia, X-Linked .
Anhydrotic Ectodermal Dysplasia, X-Linked .
CST Syndrome .
Ectodermal Dysplasia 1 .
Ectodermal Dysplasia 1, Anhydrotic .
Ectodermal Dysplasia, Anhidrotic, X-Linked .
Ectodermal Dysplasia, Hypohidrotic, X-Linked .
Ectodermal Dysplasia, Hypohydridic, X-Linked .
Hypohidrotic Ectodermal Dysplasia .
X-Linked Hypohydridic Ectodermal Dysplasia .
Anhidrotic Ectodermal Dysplasia, X Linked .
Anhydrotic Ectodermal Dysplasia, X Linked .
CST Syndromes .
Christ Siemens Touraine Syndrome .
Dysplasia 1, Ectodermal .
Ectodermal Dysplasia 1s .
Syndrome, CST .
Syndromes, CST .
X Linked Hypohydridic Ectodermal Dysplasia .
Christ-Siemens-Touraine Syndrome .
X-Linked Hypohydridic Ectodermal Dysplasia .
1.00
11155
 
Tourette Syndrome .
Chronic Motor and Vocal Tic Disorder .
Combined Multiple Motor and Vocal Tic Disorder .
Combined Vocal and Multiple Motor Tic Disorder .
Gilles De La Tourette's Syndrome .
Gilles de la Tourette Syndrome .
Multiple Motor and Vocal Tic Disorder, Combined .
Tourette Disease .
Tourette Disorder .
Tourette's Disease .
Tourette's Disorder .
Tourette's Syndrome .
Syndrome, Tourette .
Tourettes Disease .
Tourettes Disorder .
Tourettes Syndrome .
Gilles de la Tourette's Disease .
Tic Disorder, Combined Vocal and Multiple Motor .
TOURETTE'S DISORDER .
0.56
1053924
 
Incontinentia Pigmenti .
Bloch-Siemens Syndrome .
Bloch-Siemens-Sulzberger Syndrome .
Bloch Sulzberger Syndrome .
Syndrome, Bloch-Sulzberger .
Bloch-Sulzberger Syndrome .
0.55
62555
 
Osteoarthropathy, Primary Hypertrophic .
Acropachy, Hereditary .
Clubbing of Digits .
Cranioosteoarthropathy .
Currarino Idiopathic Osteoarthropathy .
Digital Clubbing, Isolated Congenital .
Familial Idiopathic Osteoarthropathy Of Childhood .
Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant .
Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive .
Idiopathic Hypertrophic Osteoarthropathy .
Pachydermoperiostosis, Autosomal Dominant .
Pachydermoperiostosis, Autosomal Recessive .
Primary Hypertrophic Osteoarthropathy, Autosomal Dominant .
Touraine-Solente-Gole Syndrome .
Acropachies, Hereditary .
Autosomal Dominant Pachydermoperiostoses .
Autosomal Dominant Pachydermoperiostosis .
Autosomal Recessive Pachydermoperiostosis .
Cranioosteoarthropathies .
Hereditary Acropachies .
Hereditary Acropachy .
Hypertrophic Osteoarthropathy, Idiopathic .
Hypertrophic Osteoarthropathy, Primary .
Osteoarthropathy, Currarino Idiopathic .
Osteoarthropathy, Idiopathic Hypertrophic .
Pachydermoperiostoses, Autosomal Dominant .
Primary Hypertrophic Osteoarthropathy .
Recessive Pachydermoperiostosis, Autosomal .
Touraine Solente Gole Syndrome .
Pachydermoperiostosis .
0.51
41572
 
Kartagener Syndrome .
Ciliary Dyskinesia, Primary, 1 .
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus .
Dextrocardia, Bronchiectasis, and Sinusitis .
Kartagener's Syndrome .
Kartagener's Triad .
Polynesian Bronchiectasis .
Primary Ciliary Dyskinesia .
Siewert Syndrome .
Bronchiectasis, Polynesian .
Dyskinesia, Primary Ciliary .
Kartageners Syndrome .
Kartageners Triad .
Polynesian Bronchiectases .
Syndrome, Kartagener .
Syndrome, Kartagener's .
Syndrome, Siewert .
Ciliary Dyskinesia, Primary .
Kartagener Triad .
KARTAGENER'S SYNDROME .
KARTAGENER'S TRIAD .
0.48
581091