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 DeCS Categories

C09 Otorhinolaryngologic Diseases .
C09.218 Ear Diseases .
C09.218.568 Labyrinth Diseases .
C09.218.568.900 Vestibular Diseases .
C09.218.568.900.442 Bilateral Vestibulopathy .
C10 Nervous System Diseases .
C10.500 Nervous System Malformations .
C10.500.300 Hereditary Sensory and Motor Neuropathy .
C10.500.300.200 Charcot-Marie-Tooth Disease .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.495 Hereditary Sensory and Motor Neuropathy .
C10.574.500.495.200 Charcot-Marie-Tooth Disease .
C10.597 Neurologic Manifestations .
C10.597.057 Bilateral Vestibulopathy .
C10.597.704 Reflex, Abnormal .
C10.668 Neuromuscular Diseases .
C10.668.829 Peripheral Nervous System Diseases .
C10.668.829.800 Polyneuropathies .
C10.668.829.800.300 Hereditary Sensory and Motor Neuropathy .
C10.668.829.800.300.200 Charcot-Marie-Tooth Disease .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.666 Nervous System Malformations .
C16.131.666.300 Hereditary Sensory and Motor Neuropathy .
C16.131.666.300.200 Charcot-Marie-Tooth Disease .
C16.320 Genetic Diseases, Inborn .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.375 Hereditary Sensory and Motor Neuropathy .
C16.320.400.375.200 Charcot-Marie-Tooth Disease .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.057 Bilateral Vestibulopathy .
C23.888.592.717 Reflex, Abnormal .
E01 Diagnosis .
E01.370 Diagnostic Techniques and Procedures .
E01.370.376 Diagnostic Techniques, Neurological .
E01.370.376.550 Neurologic Examination .
E01.370.376.550.650 Reflex .
E01.370.376.550.650.655 Reflex, Abnormal .
E01.370.600 Physical Examination .
E01.370.600.550 Neurologic Examination .
E01.370.600.550.650 Reflex .
E01.370.600.550.650.655 Reflex, Abnormal .
F02 Psychological Phenomena .
F02.830 Psychophysiology .
F02.830.702 Reflex .
G11 Musculoskeletal and Neural Physiological Phenomena .
G11.561 Nervous System Physiological Phenomena .
G11.561.731 Reflex .
G11.561.731.587 Reflex, Abnormal .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Reflex, Abnormal .
Abnormal Deep Tendon Reflex .
Abnormal Reflex .
Abnormal Reflexes .
Bulbocavernosus Reflex, Decreased .
Bulbocavernousus Reflex Absent .
Hoffman's Reflex .
Palmo-Mental Reflex .
Reflex, Absent .
Reflex, Acoustic, Abnormal .
Reflex, Anal, Absent .
Reflex, Anal, Decreased .
Reflex, Ankle, Abnormal .
Reflex, Ankle, Absent .
Reflex, Ankle, Decreased .
Reflex, Biceps, Abnormal .
Reflex, Biceps, Absent .
Reflex, Biceps, Decreased .
Reflex, Corneal, Absent .
Reflex, Corneal, Decreased .
Reflex, Decreased .
Reflex, Deep Tendon, Abnormal .
Reflex, Deep Tendon, Absent .
Reflex, Gag, Absent .
Reflex, Gag, Decreased .
Reflex, Knee, Abnormal .
Reflex, Knee, Decreased .
Reflex, Moro, Asymmetric .
Reflex, Pendular .
Reflex, Triceps, Abnormal .
Reflex, Triceps, Absent .
Reflex, Triceps, Decreased .
Reflexes, Abnormal .
Absent Reflex .
Decreased Bulbocavernosus Reflex .
Decreased Reflex .
Palmo Mental Reflex .
Pendular Reflex .
Reflex Absent, Bulbocavernousus .
Reflex, Decreased Bulbocavernosus .
Reflex, Hoffman's .
Reflex, Palmo-Mental .
Hyperreflexia .
Hyporeflexia .
AREFLEXIA .
An abnormal response to a stimulus applied to the sensory components of the nervous system. This may take the form of increased, decreased, or absent reflexes. .
1.00
454437
 
Bilateral Vestibulopathy .
Bilateral Vestibular Deficiency .
Bilateral Vestibular Insufficiency .
Bilateral Vestibular Loss .
Vestibular Areflexia .
Vestibular Deficiency, Bilateral .
Vestibular Insufficiency, Bilateral .
Vestibular Loss, Bilateral .
Vestibulopathy, Bilateral .
Impairment of the vestibular function of both inner ears which can cause difficulties with balance, gait, VERTIGO, and visual blurring. .
0.69
310
 
Reflex .
An involuntary movement or exercise of function in a part, excited in response to a stimulus applied to the periphery and transmitted to the brain or spinal cord. .
0.52
12328106
 
Charcot-Marie-Tooth Disease .
Charcot-Marie Disease .
Charcot-Marie-Tooth Disease, Autosomal Dominant, With Focally Folded Myelin Sheaths, Type 1A .
Charcot-Marie-Tooth Disease, Autosomal Dominant, with Focally Folded Myelin Sheaths, Type 1B .
Charcot-Marie-Tooth Disease, Demyelinating, Type 1A .
Charcot-Marie-Tooth Disease, Demyelinating, Type 1B .
Charcot-Marie-Tooth Disease, Slow Nerve Conduction Type, Linked To Duffy .
Charcot-Marie-Tooth Disease, Type 1A .
Charcot-Marie-Tooth Disease, Type 1B .
Charcot-Marie-Tooth Disease, Type I .
Charcot-Marie-Tooth Disease, Type IA .
Charcot-Marie-Tooth Disease, Type IB .
Charcot-Marie-Tooth Disease, Type II .
Charcot-Marie-Tooth Hereditary Neuropathy .
Charcot-Marie-Tooth Neuropathy, Type 1A .
Charcot-Marie-Tooth Neuropathy, Type 1B .
Charcot-Marie-Tooth Syndrome .
HMN Distal Type I .
HMSN 1A .
HMSN 1B .
HMSN I .
HMSN IA .
HMSN IB .
HMSN II .
HMSN1A .
HMSN1B .
Hereditary Areflexic Dystasia .
Hereditary Motor And Sensory Neuropathy IB .
Hereditary Motor and Sensory Neuropathy 1A .
Hereditary Motor and Sensory Neuropathy 1B .
Hereditary Motor and Sensory Neuropathy IA .
Hereditary Type I Motor and Sensory Neuropathy .
Neuropathy, Type I Hereditary Motor and Sensory .
Neuropathy, Type II Hereditary Motor and Sensory .
Roussy Levy Hereditary Areflexic Dystasia .
Roussy-Levy Disease .
Roussy-Levy Hereditary Areflexic Dystasia .
Areflexic Dystasia, Hereditary .
Areflexic Dystasias, Hereditary .
Atrophies, Peroneal Muscular .
Atrophy, Peroneal Muscular .
Charcot Marie Disease .
Charcot Marie Tooth Disease .
Charcot Marie Tooth Disease, Type 1A .
Charcot Marie Tooth Disease, Type 1B .
Charcot Marie Tooth Disease, Type I .
Charcot Marie Tooth Disease, Type IA .
Charcot Marie Tooth Disease, Type IB .
Charcot Marie Tooth Disease, Type II .
Charcot Marie Tooth Hereditary Neuropathy .
Charcot Marie Tooth Neuropathy, Type 1A .
Charcot Marie Tooth Neuropathy, Type 1B .
Charcot Marie Tooth Syndrome .
Dystasia, Hereditary Areflexic .
Dystasias, Hereditary Areflexic .
Hereditary Areflexic Dystasias .
Hereditary Motor and Sensory Neuropathy Type II .
Hereditary Neuropathy, Charcot-Marie-Tooth .
Muscular Atrophies, Peroneal .
Peroneal Muscular Atrophies .
Roussy Levy Disease .
Roussy Levy Syndrome .
Syndrome, Charcot-Marie-Tooth .
Syndrome, Roussy-Levy .
Atrophy, Muscular, Peroneal .
Muscular Atrophy, Peroneal .
Peroneal Muscular Atrophy .
Hereditary Motor, and Sensory Neuropathy Type I .
Hereditary Motor and Sensory-Neuropathy Type II .
HMSN Type I .
HMSN Type II .
Roussy-Levy Syndrome .
HERDITARY MOTOR, AND SENSORY NEUROPATHY TYPE I .
HMN DISTAL TYPE I .
HEREDITARY TYPE I MOTOR AND SENSORY NEUROPATHY .
NEUROPATHY, TYPE I HEREDITARY MOTOR AND SENSORY .
CHARCOT-MARIE DISEASE .
A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343) .
0.51
543313