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 Categorias DeCS

C09 Otorhinolaryngologic Diseases .
C09.218 Ear Diseases .
C09.218.458 Hearing Disorders .
C09.218.458.341 Hearing Loss .
C09.218.458.341.186 Deafness .
C09.218.458.341.186.500 Deaf-Blind Disorders .
C09.218.458.341.186.500.750 Wolfram Syndrome .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.079 Basal Ganglia Diseases .
C10.228.140.079.862 Parkinsonian Disorders .
C10.228.662 Movement Disorders .
C10.228.662.600 Parkinsonian Disorders .
C10.292 Cranial Nerve Diseases .
C10.292.700 Optic Nerve Diseases .
C10.292.700.225 Optic Atrophy .
C10.292.700.225.500 Optic Atrophies, Hereditary .
C10.292.700.225.500.980 Wolfram Syndrome .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.662 Optic Atrophies, Hereditary .
C10.574.500.662.980 Wolfram Syndrome .
C10.597 Neurologic Manifestations .
C10.597.751 Sensation Disorders .
C10.597.751.418 Hearing Disorders .
C10.597.751.418.341 Hearing Loss .
C10.597.751.418.341.186 Deafness .
C10.597.751.418.341.186.500 Deaf-Blind Disorders .
C10.597.751.418.341.186.500.750 Wolfram Syndrome .
C10.597.751.941 Vision Disorders .
C10.597.751.941.162 Blindness .
C10.597.751.941.162.625 Deaf-Blind Disorders .
C10.597.751.941.162.625.750 Wolfram Syndrome .
C11 Eye Diseases .
C11.270 Eye Diseases, Hereditary .
C11.270.564 Optic Atrophies, Hereditary .
C11.270.564.980 Wolfram Syndrome .
C11.640 Optic Nerve Diseases .
C11.640.451 Optic Atrophy .
C11.640.451.451 Optic Atrophies, Hereditary .
C11.640.451.451.980 Wolfram Syndrome .
C11.966 Vision Disorders .
C11.966.075 Blindness .
C11.966.075.375 Deaf-Blind Disorders .
C11.966.075.375.750 Wolfram Syndrome .
C12 Male Urogenital Diseases .
C12.777 Urologic Diseases .
C12.777.419 Kidney Diseases .
C12.777.419.135 Diabetes Insipidus .
C12.777.419.135.875 Wolfram Syndrome .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.351 Female Urogenital Diseases .
C13.351.968 Urologic Diseases .
C13.351.968.419 Kidney Diseases .
C13.351.968.419.135 Diabetes Insipidus .
C13.351.968.419.135.875 Wolfram Syndrome .
C14 Cardiovascular Diseases .
C14.280 Heart Diseases .
C14.280.067 Arrhythmias, Cardiac .
C14.280.067.780 Pre-Excitation Syndromes .
C14.280.067.780.977 Wolff-Parkinson-White Syndrome .
C14.280.123 Cardiac Conduction System Disease .
C14.280.123.750 Pre-Excitation Syndromes .
C14.280.123.750.977 Wolff-Parkinson-White Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.299 Deaf-Blind Disorders .
C16.131.077.299.750 Wolfram Syndrome .
C16.131.077.944 Wolf-Hirschhorn Syndrome .
C16.131.240 Cardiovascular Abnormalities .
C16.131.240.400 Heart Defects, Congenital .
C16.131.240.400.980 Wolff-Parkinson-White Syndrome .
C16.131.260 Chromosome Disorders .
C16.131.260.985 Wolf-Hirschhorn Syndrome .
C16.320 Genetic Diseases, Inborn .
C16.320.180 Chromosome Disorders .
C16.320.180.985 Wolf-Hirschhorn Syndrome .
C16.320.290 Eye Diseases, Hereditary .
C16.320.290.564 Optic Atrophies, Hereditary .
C16.320.290.564.980 Wolfram Syndrome .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.630 Optic Atrophies, Hereditary .
C16.320.400.630.980 Wolfram Syndrome .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.394 Glucose Metabolism Disorders .
C18.452.394.750 Diabetes Mellitus .
C18.452.394.750.124 Diabetes Mellitus, Type 1 .
C18.452.394.750.124.960 Wolfram Syndrome .
C19 Endocrine System Diseases .
C19.246 Diabetes Mellitus .
C19.246.267 Diabetes Mellitus, Type 1 .
C19.246.267.960 Wolfram Syndrome .
C19.700 Pituitary Diseases .
C19.700.159 Diabetes Insipidus .
C19.700.159.875 Wolfram Syndrome .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Wolff-Parkinson-White Syndrome .
Anomalous Ventricular Excitation Syndrome .
Auriculoventricular Accessory Pathway Syndrome .
False Bundle-Branch Block Syndrome .
Ventricular Pre-Excitation with Arrhythmia .
Wolf-Parkinson-White Syndrome .
Syndrome, WPW .
Syndrome, Wolf-Parkinson-White .
Syndrome, Wolff-Parkinson-White .
Wolf Parkinson White Syndrome .
Wolff Parkinson White Syndrome .
WPW Syndrome .
1.00
 
Wolf-Hirschhorn Syndrome .
4p Deletion Syndrome .
4p- Syndrome .
Chromosome 4p Deletion Syndrome .
Chromosome 4p Monosomy .
Chromosome 4p Syndrome .
Del(4p) Syndrome .
Mental Retardation, Unusual Facies, And Intrauterine Growth Retardation .
Partial Monosomy 4p .
Pitt Syndrome .
Pitt-Rogers-Danks Syndrome .
Wolf Syndrome .
Wolf-Hirchhorn Syndrome .
4p Syndrome, Chromosome .
4p Syndromes, Chromosome .
Chromosome 4p Syndromes .
Pitt Rogers Danks Syndrome .
Pitt Syndromes .
Syndrome, Chromosome 4p .
Syndrome, Pitt .
Syndrome, Pitt-Rogers-Danks .
Syndrome, Wolf .
Syndrome, Wolf-Hirchhorn .
Syndrome, Wolf-Hirschhorn .
Syndromes, Chromosome 4p .
Syndromes, Pitt .
Wolf Hirchhorn Syndrome .
Wolf Hirschhorn Syndrome .
Wolf-Hirchhorn Syndrome .
0.67
 
Parkinsonian Disorders .
Autosomal Dominant Juvenile Parkinson Disease .
Autosomal Dominant Juvenile Parkinsonism .
Autosomal Dominant Parkinsonism .
Autosomal Recessive Juvenile Parkinson Disease .
Autosomal Recessive Parkinsonism .
Autosomal Recesssive Juvenile Parkinsonism .
Chromosome 6-Linked Autosomal Recessive Parkinsonism .
Experimental Parkinson Disease .
Experimental Parkinsonism .
Experimental Parkinsonism, MPTP-Induced .
Familial Parkinson Disease, Autosomal Recessive .
Juvenile Parkinson Disease .
Juvenile Parkinson Disease, Autosomal Dominant .
Juvenile Parkinson Disease, Autosomal Recessive .
Juvenile Parkinsonism, Autosomal Dominant .
Juvenile Parkinsonism, Autosomal Recessive .
MPTP-Induced Experimental Parkinsonism .
Parkinson Disease 2 .
Parkinson Disease 2, Autosomal Recessive Juvenile .
Parkinson Disease Autosomal Recessive, Early Onset .
Parkinson Disease, Autosomal Dominant. Juvenile .
Parkinson Disease, Experimental .
Parkinson Disease, Familial, Autosomal Recessive .
Parkinson Disease, Juvenile .
Parkinson Disease, Juvenile, Autosomal Dominant .
Parkinson Disease, Juvenile, Autosomal Recessive .
Parkinsonian Diseases .
Parkinsonian Syndromes .
Parkinsonism, Early Onset, with Diurnal Fluctuation .
Parkinsonism, Early-Onset, With Diurnal Fluctuation .
Parkinsonism, Juvenile, Autosomal Dominant .
Parkinsonism, Juvenile, Autosomal Recessive .
Chromosome 6 Linked Autosomal Recessive Parkinsonism .
Diseases, Experimental Parkinson .
Dominant Parkinsonism, Autosomal .
Experimental Parkinson Diseases .
Experimental Parkinsonism, MPTP Induced .
Experimental Parkinsonisms .
Juvenile Parkinsonism .
Juvenile Parkinsonism, Familial .
Juvenile Parkinsonisms .
MPTP Induced Experimental Parkinsonism .
Parkinson Diseases, Experimental .
Parkinsonism, Autosomal Dominant .
Parkinsonism, Autosomal Recessive .
Parkinsonism, Familial Juvenile .
Parkinsonism, MPTP-Induced Experimental .
Parkinsonisms, Experimental .
Parkinsonisms, Juvenile .
Recessive Parkinsonism, Autosomal .
Familial Juvenile Parkinsonism .
Parkinsonian Syndrome .
Parkinsonism .
Parkinsonism, Experimental .
Parkinsonism, Juvenile .
Ramsay Hunt Paralysis Syndrome .
0.60
 
Wolfram Syndrome .
DIDMOADUD .
Diabetes Insipidus and Mellitus with Optic Atrophy and Deafness .
Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness .
Wolfram Syndrome 1 .
Syndrome, Wolfram .
DIDMOAD .
DIDMOAD Syndrome .
0.60