serw-MX  [xml]  
 


    
 DeCS Categories

B01 Eukaryota .
B01.650 Plants .
B01.650.940 Viridiplantae .
B01.650.940.800 Streptophyta .
B01.650.940.800.575 Embryophyta .
B01.650.940.800.575.912 Tracheophyta .
B01.650.940.800.575.912.250 Magnoliopsida .
B01.650.940.800.575.912.250.715 Meliaceae .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.854 Spinal Cord Diseases .
C10.228.854.139 Amyotrophic Lateral Sclerosis .
C10.574 Neurodegenerative Diseases .
C10.574.562 Motor Neuron Disease .
C10.574.562.250 Amyotrophic Lateral Sclerosis .
C10.574.950 TDP-43 Proteinopathies .
C10.574.950.050 Amyotrophic Lateral Sclerosis .
C10.668 Neuromuscular Diseases .
C10.668.467 Motor Neuron Disease .
C10.668.467.250 Amyotrophic Lateral Sclerosis .
C11 Eye Diseases .
C11.675 Orbital Diseases .
C11.675.349 Exophthalmos .
C11.675.349.500 Graves Disease .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.845 Proteostasis Deficiencies .
C18.452.845.800 TDP-43 Proteinopathies .
C18.452.845.800.050 Amyotrophic Lateral Sclerosis .
C19 Endocrine System Diseases .
C19.874 Thyroid Diseases .
C19.874.283 Goiter .
C19.874.283.605 Graves Disease .
C19.874.397 Hyperthyroidism .
C19.874.397.370 Graves Disease .
C20 Immune System Diseases .
C20.111 Autoimmune Diseases .
C20.111.555 Graves Disease .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.288 Disease .
D08 Enzymes and Coenzymes .
D08.811 Enzymes .
D08.811.277 Hydrolases .
D08.811.277.151 Aminohydrolases .
D08.811.277.151.350 Guanine Deaminase .
HP1 Homeopathy .
HP1.007 Homeopathic Philosophy .
HP1.007.262 Patients .
HP1.007.262.808 Disease .
HP2 Homeopathic Clinics .
HP2.029 Disease .
SP5 Epidemiology and Biostatistics .
SP5.001 Epidemiology .
SP5.001.002 Health-Disease Process .
SP5.001.002.013 Disease .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Amyotrophic Lateral Sclerosis .
ALS (Amyotrophic Lateral Sclerosis) .
Amyotrophic Lateral Sclerosis With Dementia .
Amyotrophic Lateral Sclerosis, Guam Form .
Amyotrophic Lateral Sclerosis, Parkinsonism-Dementia Complex of Guam .
Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Complex 1 .
Charcot Disease .
Dementia With Amyotrophic Lateral Sclerosis .
Gehrig's Disease .
Guam Disease .
Guam Form of Amyotrophic Lateral Sclerosis .
Lou Gehrig's Disease .
Lou-Gehrigs Disease .
Amyotrophic Lateral Sclerosis Parkinsonism Dementia Complex 1 .
Amyotrophic Lateral Sclerosis, Parkinsonism Dementia Complex of Guam .
Disease, Guam .
Disease, Lou-Gehrigs .
Gehrig Disease .
Gehrigs Disease .
Sclerosis, Amyotrophic Lateral .
Lou Gehrig Disease .
Motor Neuron Disease, Amyotrophic Lateral Sclerosis .
GEHRIG'S DISEASE .
LOU GEHRIG'S DISEASE .
A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94) .
1.00
19015442
 
Disease .
Diseases .
Illness .
Disease Concept Evolution .
A definite pathologic process with a characteristic set of signs and symptoms. It may affect the whole body or any of its parts, and its etiology, pathology, and prognosis may be known or unknown. .
0.64
93017203
 
Genetic Diseases, Inborn .
Genetic Diseases .
Genetic Disorders .
Hereditary Disease .
Inborn Genetic Diseases .
Single-Gene Defects .
Defect, Single-Gene .
Defects, Single-Gene .
Disease, Genetic .
Disease, Hereditary .
Disease, Inborn Genetic .
Diseases, Genetic .
Diseases, Hereditary .
Diseases, Inborn Genetic .
Disorder, Genetic .
Disorders, Genetic .
Genetic Disease .
Genetic Disease, Inborn .
Genetic Disorder .
Inborn Genetic Disease .
Single Gene Defects .
Single-Gene Defect .
Hereditary Diseases .
Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. .
0.55
37012779
 
Meliaceae .
Carapa .
Swietenia .
Turraea .
Carapas .
Dysoxylums .
Guareas .
Khayas .
Sandoricums .
Swietenias .
Trichilias .
Turraeas .
Dysoxylum .
Guarea .
Khaya .
Sandoricum .
Trichilia .
The mahogany plant family of the order Sapindales, subclass Rosidae, class Magnoliopsida. .
0.53
49725
 
Graves Disease .
Basedow Disease .
Hyperthyroidism, Autoimmune .
Basedows Disease .
Disease, Basedow .
Disease, Basedow's .
Disease, Graves .
Disease, Graves' .
Exophthalmic Goiters .
Goiters, Exophthalmic .
Basedow's Disease .
Exophthalmic Goiter .
Goiter, Exophthalmic .
Graves' Disease .
A common form of hyperthyroidism with a diffuse hyperplastic GOITER. It is an autoimmune disorder that produces antibodies against the THYROID STIMULATING HORMONE RECEPTOR. These autoantibodies activate the TSH receptor, thereby stimulating the THYROID GLAND and hypersecretion of THYROID HORMONES. These autoantibodies can also affect the eyes (GRAVES OPHTHALMOPATHY) and the skin (Graves dermopathy). .
0.53
33613528
 
Guanine Deaminase .
Aminase, Guanine .
Aminohydrolase, Guanine .
Deaminase, Guanine .
Guanase .
Guanine Aminase .
Guanine Aminohydrolase .
An enzyme that catalyzes the deamination of guanine to form xanthine. EC 3.5.4.3. .
0.52
2223