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Hereditary Motor and Sensory Neuropathies
Hierarchy: | ∟ ∟ ∟ ∟ Hereditary Motor and Sensory Neuropathies 39 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hereditary Motor and Sensory Neuropathies 39 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hereditary Motor and Sensory Neuropathies 39 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hereditary Motor and Sensory Neuropathies 39 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hereditary Motor and Sensory Neuropathies 39 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Broader terms: | ∟ ∟ ∟ ∟ Hereditary Motor and Sensory Neuropathies ∟ ∟ ∟ ∟ Hereditary Motor and Sensory Neuropathies ∟ ∟ ∟ Hereditary Motor and Sensory Neuropathies ∟ ∟ ∟ ∟ Hereditary Motor and Sensory Neuropathies ∟ ∟ ∟ ∟ ∟ Hereditary Motor and Sensory Neuropathies |
Narrower terms: | |
Annotation: | do not confuse with HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES; DF: NEUROPATHIES HEREDITARY MOTOR SENSORY
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History note: | Charcot-Marie Disease (1975-1988) | Muscular Atrophy (1972-1988) | Neuromuscular Diseases (1979-1988)X |
historyNote*: | 2000(1989)
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publicMeSHNote*: | 2000; see NEUROPATHIES, HEREDITARY MOTOR AND SENSORY 1988-1999
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Scope note: | 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)
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activeMeSHYear*: | |
dateCreated*: | 1999-11-08X |
dateEstablished*: | 1988-01-01X |
dateRevised*: | 2005-07-28X |
recordAuthorizer*: | agsX |
recordMaintainer*: | agsX |
recordOriginator*: | ECX |
Type: | |
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URI: | |
Labels and equivalent concepts: | Perinnölliset motoriset ja sensoriset neuropatiat (fi) XNeuropathies, Hereditary Motor and Sensory (en, replaced) HMSN Type VII (en, replaced) HMSN (en, replaced) Hereditary, Type III, Motor and Sensory Neuropathy (en, replaced) Dejerine-Sottas Disease (en, replaced) Neuropatías Motoras y Sensoriales Hereditarias (es) κληρονομικές κινητικές και αισθητικές νευροπάθειες (el) Hereditäre motorische und sensorische Neuropathien (de) dědičné motorické a senzorické neuropatie (cs) HMSN (es, replaced) Enfermedad de Dejerine-Sottas (es, replaced) HMSN Tipo III (es, replaced) HMSN Tipo VII (es, replaced) Neuropatias Hereditarias Motoras y Sensoriales (es, replaced) Neuropatía Motora y Sensorial Hereditaria Tipo VII (es, replaced) Neuropatía Motora y Sensorial Hereditaria Tipo III (es, replaced) HMSN (de, replaced) Hereditäre motorische und sensorische Neuropathie, Typ VII (de, replaced) Hereditäre motorische und sensorische Neuropathie, Typ III (de, replaced) HMSN Typ III (de, replaced) HMSN Typ VII (de, replaced) Neuropathien, hereditäre motorische und sensorische (de, replaced) Déjerine-Sottas-Krankheit (de, replaced) |
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