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 Categorias DeCS

C10 Nervous System Diseases .
C10.177 Autonomic Nervous System Diseases .
C10.177.350 Horner Syndrome .
C10.597 Neurologic Manifestations .
C10.597.690 Pupil Disorders .
C10.597.690.362 Miosis .
C10.597.690.362.500 Horner Syndrome .
C11 Eye Diseases .
C11.710 Pupil Disorders .
C11.710.528 Miosis .
C11.710.528.500 Horner Syndrome .
C15 Hemic and Lymphatic Diseases .
C15.378 Hematologic Diseases .
C15.378.100 Blood Coagulation Disorders .
C15.378.100.100 Blood Coagulation Disorders, Inherited .
C15.378.100.100.080 Bernard-Soulier Syndrome .
C15.378.140 Blood Platelet Disorders .
C15.378.140.120 Bernard-Soulier Syndrome .
C15.378.463 Hemorrhagic Disorders .
C15.378.463.080 Bernard-Soulier Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.099 Blood Coagulation Disorders, Inherited .
C16.320.099.080 Bernard-Soulier 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 .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.708 Pupil Disorders .
C23.888.592.708.362 Miosis .
C23.888.592.708.362.500 Horner Syndrome .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Horner Syndrome .
Bernard's Syndrome .
Claude Bernard-Horner Syndrome .
Horner Syndrome, Acquired .
Horner Syndrome, Central .
Horner's Syndrome, Pupil .
Ophthalmoplegia, Sympathetic Ocular .
Ptosis Sympathetic .
Sympathetic Ocular-Ophthalmoplegia .
Acquired Horner Syndrome .
Bernard Syndromes .
Bernards Syndrome .
Central Horner Syndrome .
Claude Bernard Horner Syndrome .
Horner Syndrome, Pupil .
Horners Syndrome .
Horners Syndrome, Pupil .
Ocular Ophthalmoplegia, Sympathetic .
Ocular Ophthalmoplegias, Sympathetic .
Ocular-Ophthalmoplegia, Sympathetic .
Ocular-Ophthalmoplegias, Sympathetic .
Oculosympathetic Syndromes .
Ophthalmoplegias, Sympathetic Ocular .
Pupil Horner's Syndrome .
Sympathetic Ocular Ophthalmoplegia .
Sympathetic Ocular Ophthalmoplegias .
Sympathetic Ocular-Ophthalmoplegias .
Syndrome, Acquired Horner .
Syndrome, Bernard .
Syndrome, Bernard's .
Syndrome, Central Horner .
Syndrome, Claude Bernard-Horner .
Syndrome, Horner .
Syndrome, Horner's .
Syndrome, Oculosympathetic .
Syndrome, Pupil Horner's .
Syndromes, Bernard .
Syndromes, Oculosympathetic .
Bernard Syndrome .
Horner's Syndrome .
Miosis, Innervational Defect .
Oculosympathetic Syndrome .
BERNARD'S SYNDROME .
1.00
 
Bernard-Soulier Syndrome .
Deficiency of Platelet Glycoprotein 1b .
Glycoprotein Ib, Platelet, Deficiency Of .
Platelet Glycoprotein 1b, Deficiency of .
Platelet Glycoprotein Ib Deficiency .
Von Willebrand Factor Receptor Deficiency .
Bernard Soulier Syndrome .
Platelet Syndromes, Giant .
Syndrome, Bernard-Soulier .
Syndrome, Giant Platelet .
Syndromes, Giant Platelet .
Giant Platelet Syndrome .
0.78
 
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 .
0.74