DISEASES Nervous System Diseases [C10] Nervous System Diseases Nervous System Malformations [C10.500] Nervous System Malformations Agenesis of Corpus Callosum [C10.500.034] Agenesis of Corpus Callosum Central Nervous System Cysts [C10.500.142] Central Nervous System Cysts Central Nervous System Vascular Malformations [C10.500.190] Central Nervous System Vascular Malformations Congenital Cranial Dysinnervation Disorders [C10.500.198] Congenital Cranial Dysinnervation Disorders Dandy-Walker Syndrome [C10.500.205] Dandy-Walker Syndrome Hereditary Sensory and Autonomic Neuropathies [C10.500.250] Hereditary Sensory and Autonomic Neuropathies Hereditary Sensory and Motor Neuropathy [C10.500.300] Hereditary Sensory and Motor Neuropathy Alstrom Syndrome [C10.500.300.099] Alstrom Syndrome Charcot-Marie-Tooth Disease [C10.500.300.200] Charcot-Marie-Tooth Disease Giant Axonal Neuropathy [C10.500.300.490] Giant Axonal Neuropathy Refsum Disease [C10.500.300.780] Refsum Disease Spastic Paraplegia, Hereditary [C10.500.300.820] Spastic Paraplegia, Hereditary Hydranencephaly [C10.500.450] Hydranencephaly Malformations of Cortical Development [C10.500.507] Malformations of Cortical Development Neural Tube Defects [C10.500.680] Neural Tube Defects Optic Nerve Hypoplasia [C10.500.760] Optic Nerve Hypoplasia DISEASES Nervous System Diseases [C10] Nervous System Diseases Neurodegenerative Diseases [C10.574] Neurodegenerative Diseases Heredodegenerative Disorders, Nervous System [C10.574.500] Heredodegenerative Disorders, Nervous System Alexander Disease [C10.574.500.024] Alexander Disease Amyloid Neuropathies, Familial [C10.574.500.050] Amyloid Neuropathies, Familial Bulbo-Spinal Atrophy, X-Linked [C10.574.500.175] Bulbo-Spinal Atrophy, X-Linked Canavan Disease [C10.574.500.300] Canavan Disease Cockayne Syndrome [C10.574.500.362] Cockayne Syndrome Dystonia Musculorum Deformans [C10.574.500.393] Dystonia Musculorum Deformans Gerstmann-Straussler-Scheinker Disease [C10.574.500.425] Gerstmann-Straussler-Scheinker Disease Hepatolenticular Degeneration [C10.574.500.487] Hepatolenticular Degeneration Hereditary Central Nervous System Demyelinating Diseases [C10.574.500.490] Hereditary Central Nervous System Demyelinating Diseases Hereditary Sensory and Autonomic Neuropathies [C10.574.500.493] Hereditary Sensory and Autonomic Neuropathies Hereditary Sensory and Motor Neuropathy [C10.574.500.495] Hereditary Sensory and Motor Neuropathy Alstrom Syndrome [C10.574.500.495.099] Alstrom Syndrome Charcot-Marie-Tooth Disease [C10.574.500.495.200] Charcot-Marie-Tooth Disease Giant Axonal Neuropathy [C10.574.500.495.490] Giant Axonal Neuropathy Refsum Disease [C10.574.500.495.780] Refsum Disease Spastic Paraplegia, Hereditary [C10.574.500.495.820] Spastic Paraplegia, Hereditary Huntington Disease [C10.574.500.497] Huntington Disease Lafora Disease [C10.574.500.529] Lafora Disease Myotonia Congenita [C10.574.500.545] Myotonia Congenita Myotonic Dystrophy [C10.574.500.547] Myotonic Dystrophy Neurofibromatoses [C10.574.500.549] Neurofibromatoses Neuronal Ceroid-Lipofuscinoses [C10.574.500.550] Neuronal Ceroid-Lipofuscinoses Optic Atrophies, Hereditary [C10.574.500.662] Optic Atrophies, Hereditary Pantothenate Kinase-Associated Neurodegeneration [C10.574.500.700] Pantothenate Kinase-Associated Neurodegeneration Spinal Muscular Atrophies of Childhood [C10.574.500.812] Spinal Muscular Atrophies of Childhood Spinocerebellar Degenerations [C10.574.500.825] Spinocerebellar Degenerations Tourette Syndrome [C10.574.500.850] Tourette Syndrome Tuberous Sclerosis [C10.574.500.865] Tuberous Sclerosis Unverricht-Lundborg Syndrome [C10.574.500.875] Unverricht-Lundborg Syndrome DISEASES Nervous System Diseases [C10] Nervous System Diseases Neuromuscular Diseases [C10.668] Neuromuscular Diseases Peripheral Nervous System Diseases [C10.668.829] Peripheral Nervous System Diseases Polyneuropathies [C10.668.829.800] Polyneuropathies Alcoholic Neuropathy [C10.668.829.800.050] Alcoholic Neuropathy Hereditary Sensory and Autonomic Neuropathies [C10.668.829.800.175] Hereditary Sensory and Autonomic Neuropathies Hereditary Sensory and Motor Neuropathy [C10.668.829.800.300] Hereditary Sensory and Motor Neuropathy Alstrom Syndrome [C10.668.829.800.300.099] Alstrom Syndrome Charcot-Marie-Tooth Disease [C10.668.829.800.300.200] Charcot-Marie-Tooth Disease Giant Axonal Neuropathy [C10.668.829.800.300.490] Giant Axonal Neuropathy Refsum Disease [C10.668.829.800.300.780] Refsum Disease Spastic Paraplegia, Hereditary [C10.668.829.800.300.820] Spastic Paraplegia, Hereditary Paraneoplastic Polyneuropathy [C10.668.829.800.662] Paraneoplastic Polyneuropathy POEMS Syndrome [C10.668.829.800.700] POEMS Syndrome Polyradiculoneuropathy [C10.668.829.800.750] Polyradiculoneuropathy Tangier Disease [C10.668.829.800.875] Tangier Disease DISEASES Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormalities [C16.131] Congenital Abnormalities Nervous System Malformations [C16.131.666] Nervous System Malformations Agenesis of Corpus Callosum [C16.131.666.034] Agenesis of Corpus Callosum Central Nervous System Cysts [C16.131.666.142] Central Nervous System Cysts Central Nervous System Vascular Malformations [C16.131.666.190] Central Nervous System Vascular Malformations Congenital Cranial Dysinnervation Disorders [C16.131.666.198] Congenital Cranial Dysinnervation Disorders Dandy-Walker Syndrome [C16.131.666.205] Dandy-Walker Syndrome Hereditary Sensory and Motor Neuropathy [C16.131.666.300] Hereditary Sensory and Motor Neuropathy Alstrom Syndrome [C16.131.666.300.099] Alstrom Syndrome Charcot-Marie-Tooth Disease [C16.131.666.300.200] Charcot-Marie-Tooth Disease Giant Axonal Neuropathy [C16.131.666.300.490] Giant Axonal Neuropathy Refsum Disease [C16.131.666.300.780] Refsum Disease Spastic Paraplegia, Hereditary [C16.131.666.300.820] Spastic Paraplegia, Hereditary Hereditary Sensory and Autonomic Neuropathies [C16.131.666.310] Hereditary Sensory and Autonomic Neuropathies Hydranencephaly [C16.131.666.450] Hydranencephaly Malformations of Cortical Development [C16.131.666.507] Malformations of Cortical Development Neural Tube Defects [C16.131.666.680] Neural Tube Defects Optic Nerve Hypoplasia [C16.131.666.763] Optic Nerve Hypoplasia DISEASES Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] Congenital, Hereditary, and Neonatal Diseases and Abnormalities Genetic Diseases, Inborn [C16.320] Genetic Diseases, Inborn Heredodegenerative Disorders, Nervous System [C16.320.400] Heredodegenerative Disorders, Nervous System Alexander Disease [C16.320.400.024] Alexander Disease Amyloid Neuropathies, Familial [C16.320.400.050] Amyloid Neuropathies, Familial Bulbo-Spinal Atrophy, X-Linked [C16.320.400.100] Bulbo-Spinal Atrophy, X-Linked Canavan Disease [C16.320.400.150] Canavan Disease Cockayne Syndrome [C16.320.400.200] Cockayne Syndrome Dystonia Musculorum Deformans [C16.320.400.330] Dystonia Musculorum Deformans Gerstmann-Straussler-Scheinker Disease [C16.320.400.350] Gerstmann-Straussler-Scheinker Disease Hepatolenticular Degeneration [C16.320.400.361] Hepatolenticular Degeneration Hereditary Central Nervous System Demyelinating Diseases [C16.320.400.367] Hereditary Central Nervous System Demyelinating Diseases Hereditary Sensory and Motor Neuropathy [C16.320.400.375] Hereditary Sensory and Motor Neuropathy Alstrom Syndrome [C16.320.400.375.099] Alstrom Syndrome Charcot-Marie-Tooth Disease [C16.320.400.375.200] Charcot-Marie-Tooth Disease Giant Axonal Neuropathy [C16.320.400.375.490] Giant Axonal Neuropathy Refsum Disease [C16.320.400.375.780] Refsum Disease Spastic Paraplegia, Hereditary [C16.320.400.375.820] Spastic Paraplegia, Hereditary Hereditary Sensory and Autonomic Neuropathies [C16.320.400.415] Hereditary Sensory and Autonomic Neuropathies Huntington Disease [C16.320.400.430] Huntington Disease Lafora Disease [C16.320.400.480] Lafora Disease Mental Retardation, X-Linked [C16.320.400.525] Mental Retardation, X-Linked Myotonia Congenita [C16.320.400.540] Myotonia Congenita Myotonic Dystrophy [C16.320.400.542] Myotonic Dystrophy Neuroacanthocytosis [C16.320.400.550] Neuroacanthocytosis Neurofibromatoses [C16.320.400.560] Neurofibromatoses Neuronal Ceroid-Lipofuscinoses [C16.320.400.600] Neuronal Ceroid-Lipofuscinoses Optic Atrophies, Hereditary [C16.320.400.630] Optic Atrophies, Hereditary Pantothenate Kinase-Associated Neurodegeneration [C16.320.400.650] Pantothenate Kinase-Associated Neurodegeneration Spinal Muscular Atrophies of Childhood [C16.320.400.765] Spinal Muscular Atrophies of Childhood Spinocerebellar Degenerations [C16.320.400.780] Spinocerebellar Degenerations Tourette Syndrome [C16.320.400.820] Tourette Syndrome Tuberous Sclerosis [C16.320.400.880] Tuberous Sclerosis Unverricht-Lundborg Syndrome [C16.320.400.940] Unverricht-Lundborg Syndrome

Hereditary Sensory and Motor Neuropathy - Concepto preferido

UI del concepto	M0023767
Nota de alcance	A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-TOOTH DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343)
Término preferido	Hereditary Sensory and Motor Neuropathy
Término(s) alternativo(s)	HMSN Herditary Sensory and Motor Neuropathy Hereditary Motor and Sensory Neuropathies Hereditary Motor and Sensory Neuropathy Neuropathies, Hereditary Motor and Sensory

Hereditary, Type VII, Motor and Sensory Neuropathy - Más estrecho

UI del concepto	M0336471
Término preferido	Hereditary, Type VII, Motor and Sensory Neuropathy
Término(s) alternativo(s)	HMSN Type VII HMSN Type VIIs Type VII, HMSN

HMSN Type III - Relacionado pero no más amplio ni más estrecho

UI del concepto	M0023764
Término preferido	HMSN Type III
Término(s) alternativo(s)	CMT4f Charcot Marie Tooth Disease, Type 3 Charcot-Marie-Tooth Disease, Demyelinating, Type 4f Charcot-Marie-Tooth Disease, Type 3 Dejerine Sottas Disease Dejerine Sottas Neuropathy Dejerine Sottas Syndrome Dejerine-Sottas Disease Dejerine-Sottas Hypertrophic Neuropathy Dejerine-Sottas Neuropathy Dejerine-Sottas Syndrome Disease, Dejerine-Sottas HMSN Type IIIs HMSN3 Hereditary Motor and Sensory Neuropathy 3 Hereditary Motor and Sensory Neuropathy Type III Hereditary, Type III, Motor and Sensory Neuropathy Hypertrophic Neuropathy of Dejerine Sottas Hypertrophic Neuropathy of Dejerine-Sottas Neuropathy, Dejerine-Sottas Syndrome, Dejerine-Sottas