Categorias DeCS
C07 Stomatognathic Diseases .
C07.465 Mouth Diseases .
C07.465.299 Facial Nerve Diseases .
C07.465.299.825 Mobius Syndrome .
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 .
C10.114 Autoimmune Diseases of the Nervous System .
C10.114.812 Stiff-Person Syndrome .
C10.228 Central Nervous System Diseases .
C10.228.854 Spinal Cord Diseases .
C10.228.854.790 Stiff-Person Syndrome .
C10.292 Cranial Nerve Diseases .
C10.292.319 Facial Nerve Diseases .
C10.292.319.825 Mobius Syndrome .
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 .
C10.668 Neuromuscular Diseases .
C10.668.900 Stiff-Person 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 .
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 .
C16.131.077.578 Mobius Syndrome .
C16.131.077.944 Wolf-Hirschhorn 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 .
C16.614 Infant, Newborn, Diseases .
C16.614.595 Mobius 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 .
C20 Immune System Diseases .
C20.111 Autoimmune Diseases .
C20.111.258 Autoimmune Diseases of the Nervous System .
C20.111.258.850 Stiff-Person Syndrome .
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| | Termos Sinônimos e Históricos | Documentos LILACS e MDL | |
| Stiff-Person Syndrome . Congenital Stiff-Man Syndrome . Congenital Stiff-Person Syndrome . Familial Hyperekplexia . Hereditary Hyperekplexia . Startle Syndrome . Stiff-Baby Syndrome . Stiff-Trunk Syndrome . Stiffman Syndrome . Congenital Stiff Man Syndrome . Congenital Stiff-Man Syndromes . Congenital Stiff-Person Syndromes . Familial Hyperekplexias . Hereditary Hyperekplexias . Hyperekplexia, Familial . Hyperekplexia, Hereditary . Hyperekplexias, Familial . Hyperekplexias, Hereditary . Moersch Woltmann Syndrome . Startle Syndromes . Stiff Man Syndrome . Stiff Person Syndrome . Stiff Trunk Syndrome . Stiff-Baby Syndromes . Stiff-Man Syndrome, Congenital . Stiff-Man Syndromes, Congenital . Stiff-Person Syndrome, Congenital . Stiff-Person Syndromes, Congenital . Stiff-Trunk Syndromes . Syndrome, Congenital Stiff-Man . Syndrome, Congenital Stiff-Person . Syndrome, Moersch-Woltmann . Syndrome, Startle . Syndrome, Stiff-Baby . Syndrome, Stiff-Man . Syndrome, Stiff-Person . Syndrome, Stiff-Trunk . Syndrome, Stiffman . Syndromes, Congenital Stiff-Man . Syndromes, Congenital Stiff-Person . Syndromes, Startle . Syndromes, Stiff-Baby . Syndromes, Stiff-Trunk . Moersch-Woltmann Syndrome . Stiff-Man Syndrome . 1.00
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| 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 . 0.61
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