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 .
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| | Termos Sinônimos e Históricos | Documentos LILACS e MDL | | | | |
| 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
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| 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
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