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 Categorias DeCS

C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.099 Bone Diseases, Developmental .
C05.116.099.370 Dysostoses .
C05.116.099.370.231 Craniofacial Dysostosis .
C05.116.099.370.231.576 Mandibulofacial Dysostosis .
C05.116.099.370.231.576.410 Goldenhar Syndrome .
C05.651 Muscular Diseases .
C05.651.460 Mitochondrial Myopathies .
C05.651.460.700 Ophthalmoplegia, Chronic Progressive External .
C05.651.460.700.500 Kearns-Sayre Syndrome .
C05.660 Musculoskeletal Abnormalities .
C05.660.207 Craniofacial Abnormalities .
C05.660.207.231 Craniofacial Dysostosis .
C05.660.207.231.576 Mandibulofacial Dysostosis .
C05.660.207.231.576.410 Goldenhar Syndrome .
C10 Nervous System Diseases .
C10.177 Autonomic Nervous System Diseases .
C10.177.350 Horner Syndrome .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.640 Oculocerebrorenal Syndrome .
C10.292 Cranial Nerve Diseases .
C10.292.562 Ocular Motility Disorders .
C10.292.562.750 Ophthalmoplegia .
C10.292.562.750.250 Ophthalmoplegia, Chronic Progressive External .
C10.292.562.750.250.500 Kearns-Sayre Syndrome .
C10.597 Neurologic Manifestations .
C10.597.622 Paralysis .
C10.597.622.447 Ophthalmoplegia .
C10.597.622.447.511 Ophthalmoplegia, Chronic Progressive External .
C10.597.622.447.511.500 Kearns-Sayre Syndrome .
C10.597.690 Pupil Disorders .
C10.597.690.362 Miosis .
C10.597.690.362.500 Horner Syndrome .
C10.668 Neuromuscular Diseases .
C10.668.491 Muscular Diseases .
C10.668.491.500 Mitochondrial Myopathies .
C10.668.491.500.700 Ophthalmoplegia, Chronic Progressive External .
C10.668.491.500.700.500 Kearns-Sayre Syndrome .
C11 Eye Diseases .
C11.590 Ocular Motility Disorders .
C11.590.472 Ophthalmoplegia .
C11.590.472.250 Ophthalmoplegia, Chronic Progressive External .
C11.590.472.250.500 Kearns-Sayre Syndrome .
C11.710 Pupil Disorders .
C11.710.528 Miosis .
C11.710.528.500 Horner Syndrome .
C11.768 Retinal Diseases .
C11.768.585 Retinal Degeneration .
C11.768.585.658 Retinal Dystrophies .
C11.768.585.658.500 Retinitis Pigmentosa .
C11.768.585.658.500.627 Kearns-Sayre Syndrome .
C12 Male Urogenital Diseases .
C12.777 Urologic Diseases .
C12.777.419 Kidney Diseases .
C12.777.419.815 Renal Tubular Transport, Inborn Errors .
C12.777.419.815.720 Oculocerebrorenal Syndrome .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.351 Female Urogenital Diseases .
C13.351.968 Urologic Diseases .
C13.351.968.419 Kidney Diseases .
C13.351.968.419.815 Renal Tubular Transport, Inborn Errors .
C13.351.968.419.815.720 Oculocerebrorenal Syndrome .
C14 Cardiovascular Diseases .
C14.280 Heart Diseases .
C14.280.238 Cardiomyopathies .
C14.280.238.510 Kearns-Sayre Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.662 Oculocerebrorenal Syndrome .
C16.131.621 Musculoskeletal Abnormalities .
C16.131.621.207 Craniofacial Abnormalities .
C16.131.621.207.231 Craniofacial Dysostosis .
C16.131.621.207.231.576 Mandibulofacial Dysostosis .
C16.131.621.207.231.576.410 Goldenhar Syndrome .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.750 Oculocerebrorenal Syndrome .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.151 Amino Acid Transport Disorders, Inborn .
C16.320.565.151.600 Oculocerebrorenal Syndrome .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.640 Oculocerebrorenal Syndrome .
C16.320.565.861 Renal Tubular Transport, Inborn Errors .
C16.320.565.861.750 Oculocerebrorenal Syndrome .
C16.320.709 Oculocerebrorenal Syndrome .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.640 Oculocerebrorenal Syndrome .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.151 Amino Acid Transport Disorders, Inborn .
C18.452.648.151.600 Oculocerebrorenal Syndrome .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.640 Oculocerebrorenal Syndrome .
C18.452.648.861 Renal Tubular Transport, Inborn Errors .
C18.452.648.861.750 Oculocerebrorenal Syndrome .
C18.452.660 Mitochondrial Diseases .
C18.452.660.410 Kearns-Sayre Syndrome .
C18.452.660.560 Mitochondrial Myopathies .
C18.452.660.560.700 Ophthalmoplegia, Chronic Progressive External .
C18.452.660.560.700.500 Kearns-Sayre Syndrome .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.288 Disease .
C23.550.288.500 Syndrome .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.636 Paralysis .
C23.888.592.636.447 Ophthalmoplegia .
C23.888.592.636.447.511 Ophthalmoplegia, Chronic Progressive External .
C23.888.592.636.447.511.500 Kearns-Sayre Syndrome .
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
 
Kearns-Sayre Syndrome .
CPEO with Myopathy .
CPEO with Ragged Red Fibers .
Chronic Progressive External Ophthalmoplegia with Myopathy .
Cpeo With Ragged-Red Fibers .
Kearn-Sayre Mitochondrial Cytopathy .
Kearns Sayre Syndrome .
Kearns' Syndrome .
Kearns-Sayre Mitochondrial Cytopathy .
Kearns-Sayre-Shy-Daroff Syndrome .
Oculocraniosomatic Syndrome .
Ophthalmoplegia Plus Syndrome .
Ophthalmoplegia, Pigmentary Degeneration of Retina, and Cardiomyopathy .
Ophthalmoplegia, Progressive External, With Ragged-Red Fibers .
Ophthalmoplegia-Plus Syndrome .
CPEO with Myopathies .
Cytopathy, Kearn-Sayre Mitochondrial .
Kearn Sayre Mitochondrial Cytopathy .
Kearn Syndrome .
Kearns Sayre Shy Daroff Syndrome .
Mitochondrial Cytopathy, Kearn-Sayre .
Myopathies, CPEO with .
Myopathy, CPEO with .
Oculocraniosomatic Syndromes .
Ophthalmoplegia Plus Syndromes .
Sayre Syndrome, Kearns .
Syndrome, Kearns .
Syndrome, Kearns Sayre .
Syndrome, Kearns' .
Syndrome, Kearns-Sayre .
Syndrome, Kearns-Sayre-Shy-Daroff .
Syndrome, Oculocraniosomatic .
Syndrome, Ophthalmoplegia Plus .
Kearns Syndrome .
Kearns-Sayer Syndrome .
KEARNS-SAYRE-SHY-DAROFF SYNDROME .
0.59
 
Oculocerebrorenal Syndrome .
Cerebro-Oculo-Renal Syndrome .
Lowe Disease .
Lowe Oculocerebrorenal Syndrome .
Lowe-Bickel Syndrome .
Lowe-Terrey-MacLachlan Syndrome .
Oculocerebrorenal Dystrophy .
Oculocerebrorenal Syndrome of Lowe .
Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency .
Phosphatidylinositol-4,5-Bisphosphate-5-Phosphatase Deficiency .
Renal-Oculocerebrodystrophy .
Cerebro Oculo Renal Syndrome .
Deficiency, Phosphatidylinositol-4,5-Bisphosphate-5-Phosphatase .
Dystrophy, Oculocerebrorenal .
Lowe Bickel Syndrome .
Lowe Terrey MacLachlan Syndrome .
Phosphatidylinositol 4,5 Bisphosphate 5 Phosphatase Deficiency .
Renal Oculocerebrodystrophy .
Lowe Syndrome .
Cerebrooculorenal Syndrome .
0.57
 
Goldenhar Syndrome .
Craniofacial Microsomia .
Facioauriculovertebral Dysplasia .
Facioauriculovertebral Sequence .
First and Second Branchial Arch Syndrome .
First and Second Pharyngeal Arch Syndromes .
Goldenhar Disease .
Goldenhar Syndrome with Ipsilateral Radial Defect .
Goldenhar-Gorlin Syndrome .
Hemifacial Microsomia with Radial Defects .
Lateral Facial Dysplasia .
Microsomia Hemifacial Radial Defects .
Moeschler Clarren Syndrome .
OAVS with Radial Defect .
Oculoauriculovertebral Dysplasia .
Oculoauriculovertebral Spectrum .
Oculoauriculovertebral Spectrum with Radial Defect .
Oral-Mandibular-Auricular Syndrome .
Otomandibular Dysostosis .
Craniofacial Microsomias .
Dysostosis, Otomandibular .
Dysplasia, Facioauriculovertebral .
Dysplasia, Lateral Facial .
Dysplasia, Oculoauriculovertebral .
Dysplasias, Facioauriculovertebral .
Dysplasias, Lateral Facial .
Dysplasias, Oculoauriculovertebral .
Facial Dysplasia, Lateral .
Facial Dysplasias, Lateral .
Facioauriculovertebral Dysplasias .
Facioauriculovertebral Sequences .
Goldenhar Gorlin Syndrome .
Goldenhar-Gorlin Syndromes .
Lateral Facial Dysplasias .
Microsomia, Craniofacial .
Microsomias, Craniofacial .
Oculoauriculovertebral Dysplasias .
Oculoauriculovertebral Spectrums .
Oral Mandibular Auricular Syndrome .
Oral-Mandibular-Auricular Syndromes .
Hemifacial Microsomia .
Oculoauriculovertebral Syndrome .
0.54
 
Syndrome .
Symptom Cluster .
Cluster, Symptom .
Clusters, Symptom .
Symptom Clusters .
Syndromes .
0.51