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 Categorias DeCS

C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.099 Bone Diseases, Developmental .
C05.116.099.708 Osteochondrodysplasias .
C05.116.099.708.479 Hyperostosis, Cortical, Congenital .
C05.116.540 Hyperostosis .
C05.116.540.400 Hyperostosis, Cortical, Congenital .
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 .
C16.320.728 Osteochondrodysplasias .
C16.614 Infant, Newborn, Diseases .
C16.614.465 Hyperostosis, Cortical, Congenital .
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 .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
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 .
1.00
14526
 
Osteochondrodysplasias .
Chondrodystrophic Myotonia .
Dyschondroplasia .
Endosteal Hyperostosis, Autosomal Recessive .
Hyperphosphatasemia Tarda .
Late-Onset Spondyloepiphyseal Dysplasia .
Melnick-Needles Osteodysplasty .
Myotonic Chondrodystrophy .
Myotonic Myopathy, Dwarfism, Chondrodystrophy, And Ocular And Facial Abnormalities .
Osteodysplasty of Melnick and Needles .
SED Tarda .
SJA Syndrome .
Schwartz Jampel Aberfeld syndrome .
Schwartz-Jampel Syndrome, Type 1 .
Schwartz-Jampel-Aberfeld Syndrome .
Sost Sclerosing Bone Dysplasia .
Sost-Related Sclerosing Bone Dysplasia .
Spondylo-Epimetaphyseal Dysplasia With Myotonia .
Spondyloepiphyseal Dysplasia Tarda, X-Linked .
Spondyloepiphyseal Dysplasia, Late .
Van Buchem Disease .
X-Linked SED .
X-Linked SEDT .
X-Linked Spondyloepiphyseal Dysplasia Tarda .
Chondrodystrophy, Myotonic .
Dysplasia, Spondyloepiphyseal .
Late Onset Spondyloepiphyseal Dysplasia .
Late Spondyloepiphyseal Dysplasia .
Melnick Needles Osteodysplasty .
Melnick Needles Syndrome .
Myotonia, Chondrodystrophic .
Osteochondrodysplasia .
Osteodysplasty, Melnick-Needles .
SED, X-Linked .
SEDT, X-Linked .
Schwartz Jampel Syndrome .
Schwartz Jampel Syndrome, Type 1 .
Spondyloepiphyseal Dysplasia Tarda, X Linked .
Spondyloepiphyseal Dysplasia, Late-Onset .
Syndrome, Schwartz-Jampel-Aberfeld .
X Linked SED .
X Linked SEDT .
X Linked Spondyloepiphyseal Dysplasia Tarda .
Dyschondroplasias .
Hyperostosis Corticalis Generalisata .
Melnick-Needles Syndrome .
Multiple Epiphyseal Dysplasia .
Schwartz-Jampel Syndrome .
Spondyloepiphyseal Dysplasia .
0.81
1094052
 
Hyperostosis, Cortical, Congenital .
Caffey Disease .
Congenital Hyperostosis, Cortical .
Cortical Congenital Hyperostosis .
Familial Caffey's Disease .
Familial Infantile Cortical Hyperostosis .
Caffey De Toni Silvermann Syndrome .
Caffey's Disease, Familial .
Congenital Cortical Hyperostoses .
Congenital Cortical Hyperostosis .
Congenital Hyperostoses, Cortical .
Cortical Congenital Hyperostoses .
Cortical Hyperostoses, Congenital .
Cortical Hyperostoses, Infantile .
Cortical Hyperostosis, Infantile .
Disease, Caffey .
Disease, Familial Caffey's .
Familial Caffey Disease .
Familial Caffeys Disease .
Hyperostoses, Congenital Cortical .
Hyperostoses, Cortical Congenital .
Hyperostoses, Infantile Cortical .
Hyperostosis, Congenital Cortical .
Hyperostosis, Cortical Congenital .
Hyperostosis, Infantile Cortical .
Infantile Cortical Hyperostoses .
Syndrome, Caffey-De Toni-Silvermann .
Infantile Cortical Hyperostosis .
Caffey-De Toni-Silvermann Syndrome .
Cortical Hyperostosis, Congenital .
0.55
19449