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 DeCS Categories

C04 Neoplasms .
C04.557 Neoplasms by Histologic Type .
C04.557.450 Neoplasms, Connective and Soft Tissue .
C04.557.450.565 Neoplasms, Connective Tissue .
C04.557.450.565.590 Neoplasms, Fibrous Tissue .
C04.557.450.565.590.350 Fibrosarcoma .
C04.557.450.565.590.350.320 Dermatofibrosarcoma .
C04.557.450.795 Sarcoma .
C04.557.450.795.350 Fibrosarcoma .
C04.557.450.795.350.320 Dermatofibrosarcoma .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.854 Spinal Cord Diseases .
C10.228.854.468 Muscular Atrophy, Spinal .
C10.228.854.468.800 Spinal Muscular Atrophies of Childhood .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.812 Spinal Muscular Atrophies of Childhood .
C10.574.562 Motor Neuron Disease .
C10.574.562.500 Muscular Atrophy, Spinal .
C10.574.562.500.750 Spinal Muscular Atrophies of Childhood .
C10.597 Neurologic Manifestations .
C10.597.704 Reflex, Abnormal .
C10.668 Neuromuscular Diseases .
C10.668.467 Motor Neuron Disease .
C10.668.467.500 Muscular Atrophy, Spinal .
C10.668.467.500.750 Spinal Muscular Atrophies of Childhood .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.765 Spinal Muscular Atrophies of Childhood .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
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 .
E01.370.376.550.650.680 Reflex, Babinski .
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 .
E01.370.600.550.650.680 Reflex, Babinski .
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 .
G11.561.731.618 Reflex, Babinski .
 
 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
 
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. .
0.54
12128106
 
Reflex, Babinski .
Babinski Reflexes .
Babinski Sign .
Babinski Sign Absent .
Babinski Sign Negative .
Babinski Sign Positive .
Babinski's Reflex .
Babinski's Sign .
Extensor Plantar Reflex .
Great Toe Paradoxical Extensor Reflex .
Reflexes, Babinski .
Reflex, Babinski's .
Babinski Reflex .
Extensor Plantar Response .
Paradoxical Extensor Reflex, Great Toe .
A reflex found in normal infants consisting of dorsiflexion of the HALLUX and abduction of the other TOES in response to cutaneous stimulation of the plantar surface of the FOOT. In adults, it is used as a diagnostic criterion, and if present is a NEUROLOGIC MANIFESTATION of dysfunction in the CENTRAL NERVOUS SYSTEM. .
0.48
23283
 
Dermatofibrosarcoma .
Bednar Tumor .
Bednar's Tumor .
DFSP, Fibrosarcomatous .
DFSP, Juvenile .
DFSP, Myxoid .
DFSP, Pigmented .
Darier-Ferrand Tumor .
Darier-Hoffmann Tumor .
Dermatofibrosarcoma Protuberan .
Dermatofibrosarcoma Protuberans, Familial .
Dermatofibrosarcoma Protuberans, Fibrosarcomatous .
Dermatofibrosarcoma Protuberans, Giant Cell .
Dermatofibrosarcoma Protuberans, Myxoid .
Dermatofibrosarcoma Protuberans, Pigmented .
FS-DFSP .
Familial Dermatofibrosarcoma Protuberans .
Fibrosarcomatous Dermatofibrosarcoma Protuberans .
Giant Cell Fibroblastoma .
Giant Dermatofibrosarcoma Protuberans .
Metastatic Dermatofibrosarcoma Protuberans .
Bednars Tumor .
Cell Fibroblastoma, Giant .
Cell Fibroblastomas, Giant .
DFSPs, Fibrosarcomatous .
DFSPs, Juvenile .
DFSPs, Myxoid .
DFSPs, Pigmented .
Darier Ferrand Tumor .
Darier Hoffmann Tumor .
Dermatofibrosarcoma Protuberan, Familial .
Dermatofibrosarcoma Protuberan, Fibrosarcomatous .
Dermatofibrosarcoma Protuberan, Giant .
Dermatofibrosarcoma Protuberan, Metastatic .
Dermatofibrosarcoma Protuberan, Myxoid .
Dermatofibrosarcoma Protuberan, Pigmented .
Dermatofibrosarcoma Protuberans .
Dermatofibrosarcoma Protuberans, Giant .
Dermatofibrosarcoma Protuberans, Metastatic .
Dermatofibrosarcomas .
Familial Dermatofibrosarcoma Protuberan .
Fibroblastoma, Giant Cell .
Fibroblastomas, Giant Cell .
Fibrosarcomatous DFSP .
Fibrosarcomatous DFSPs .
Fibrosarcomatous Dermatofibrosarcoma Protuberan .
Giant Cell Fibroblastomas .
Giant Dermatofibrosarcoma Protuberan .
Juvenile DFSP .
Juvenile DFSPs .
Metastatic Dermatofibrosarcoma Protuberan .
Myxoid DFSP .
Myxoid DFSPs .
Myxoid Dermatofibrosarcoma Protuberan .
Myxoid Dermatofibrosarcoma Protuberans .
Pigmented DFSP .
Pigmented DFSPs .
Pigmented Dermatofibrosarcoma Protuberan .
Pigmented Dermatofibrosarcoma Protuberans .
Protuberan, Dermatofibrosarcoma .
Protuberan, Familial Dermatofibrosarcoma .
Protuberan, Fibrosarcomatous Dermatofibrosarcoma .
Protuberan, Giant Dermatofibrosarcoma .
Protuberan, Metastatic Dermatofibrosarcoma .
Protuberan, Myxoid Dermatofibrosarcoma .
Protuberan, Pigmented Dermatofibrosarcoma .
Protuberans, Dermatofibrosarcoma .
Protuberans, Familial Dermatofibrosarcoma .
Protuberans, Fibrosarcomatous Dermatofibrosarcoma .
Protuberans, Giant Dermatofibrosarcoma .
Protuberans, Metastatic Dermatofibrosarcoma .
Protuberans, Myxoid Dermatofibrosarcoma .
Protuberans, Pigmented Dermatofibrosarcoma .
Tumor, Bednar .
Tumor, Bednar's .
Tumor, Darier-Ferrand .
Tumor, Darier-Hoffmann .
A sarcoma of the deep layers of the skin. The tumors are locally aggressive tends to recur but rarely metastatic. It can be classified into variants depending on the cell type tumors are derived from or by its characteristics: Pigmented variant from MELANIN-containing DERMAL DENDRITIC CELLS; Myxoid variant, myxoid STROMAL CELLS; Giant cell variant characterized by GIANT CELLS in the tumors; and Fibrosarcomatous variant chracterized by tumor areas histologically indistinguishable from FIBROSARCOMA. .
0.47
501092
 
Spinal Muscular Atrophies of Childhood .
HMN (Hereditary Motor Neuropathy) Proximal Type I .
Kugelberg-Welander Syndrome .
Muscular Atrophy, Infantile .
Muscular Atrophy, Juvenile .
Muscular Atrophy, Spinal, Infantile Chronic Form .
Muscular Atrophy, Spinal, Intermediate Type .
Muscular Atrophy, Spinal, Type I .
Muscular Atrophy, Spinal, Type II .
Muscular Atrophy, Spinal, Type III .
Proximal Hereditary Motor Neuropathy Type I .
SMA, Infantile Acute Form .
Spinal Muscular Atrophy 1 .
Spinal Muscular Atrophy Type 2 .
Spinal Muscular Atrophy Type I .
Spinal Muscular Atrophy Type II .
Spinal Muscular Atrophy Type III .
Spinal Muscular Atrophy, Mild Childhood and Adolescent Form .
Spinal Muscular Atrophy, Type 3 .
Spinal Muscular Atrophy, Type I .
Spinal Muscular Atrophy, Type II .
Spinal Muscular Atrophy, Type III .
Type I Spinal Muscular Atrophy .
Type II Spinal Muscular Atrophy .
Type III Spinal Muscular Atrophy .
Werdnig Hoffman Disease .
Infantile Muscular Atrophy .
Juvenile Muscular Atrophy .
Kugelberg Welander Disease .
Kugelberg Welander Syndrome .
Werdnig Hoffmann Disease .
Infantile Spinal Muscular Atrophy .
Muscular Atrophy, Spinal, Infantile .
Spinal Muscular Atrophy, Infantile .
Werdnig-Hoffmann Disease .
Juvenile Spinal Muscular Atrophy .
Kugelberg-Welander Disease .
Spinal Muscular Atrophy, Juvenile .
HMN Proximal Type I .
KUGLEBERG-WELANDER DISEASE .
A group of recessive inherited diseases that feature progressive muscular atrophy and hypotonia. They are classified as type I (Werdnig-Hoffman disease), type II (intermediate form), and type III (Kugelberg-Welander disease). Type I is fatal in infancy, type II has a late infantile onset and is associated with survival into the second or third decade. Type III has its onset in childhood, and is slowly progressive. (J Med Genet 1996 Apr:33(4):281-3) .
0.46
271060