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 DeCS Categories

C04 Neoplasms .
C04.588 Neoplasms by Site .
C04.588.322 Endocrine Gland Neoplasms .
C04.588.322.078 Adrenal Gland Neoplasms .
C04.588.322.078.265 Adrenal Cortex Neoplasms .
C04.588.322.078.265.500 Adrenocortical Adenoma .
C10 Nervous System Diseases .
C10.114 Autoimmune Diseases of the Nervous System .
C10.114.375 Demyelinating Autoimmune Diseases, CNS .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.695 Leukoencephalopathies .
C10.228.140.695.562 Demyelinating Autoimmune Diseases, CNS .
C10.314 Demyelinating Diseases .
C10.314.350 Demyelinating Autoimmune Diseases, CNS .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.449 Glycogen Storage Disease .
C16.320.565.202.449.520 Glycogen Storage Disease Type III .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.449 Glycogen Storage Disease .
C18.452.648.202.449.520 Glycogen Storage Disease Type III .
C19 Endocrine System Diseases .
C19.053 Adrenal Gland Diseases .
C19.053.098 Adrenal Cortex Diseases .
C19.053.098.265 Adrenal Cortex Neoplasms .
C19.053.098.265.500 Adrenocortical Adenoma .
C19.053.347 Adrenal Gland Neoplasms .
C19.053.347.500 Adrenal Cortex Neoplasms .
C19.053.347.500.500 Adrenocortical Adenoma .
C19.344 Endocrine Gland Neoplasms .
C19.344.078 Adrenal Gland Neoplasms .
C19.344.078.265 Adrenal Cortex Neoplasms .
C19.344.078.265.500 Adrenocortical Adenoma .
C20 Immune System Diseases .
C20.111 Autoimmune Diseases .
C20.111.258 Autoimmune Diseases of the Nervous System .
C20.111.258.250 Demyelinating Autoimmune Diseases, CNS .
C22 Animal Diseases .
C22.180 Cat Diseases .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.288 Disease .
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
 
Central Nervous System Diseases .
CNS Diseases .
Central Nervous System Disorders .
CNS Disease .
Diseases of any component of the brain (including the cerebral hemispheres, diencephalon, brain stem, and cerebellum) or the spinal cord. .
1.00
42115203
 
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. .
0.66
93017203
 
Cat Diseases .
Feline Diseases .
Cat Disease .
Disease, Cat .
Disease, Feline .
Diseases, Cat .
Diseases, Feline .
Feline Disease .
Diseases of the domestic cat (Felis catus or F. domesticus). This term does not include diseases of the so-called big cats such as CHEETAHS; LIONS; tigers, cougars, panthers, leopards, and other Felidae for which the heading CARNIVORA is used. .
0.59
15319554
 
Adrenocortical Adenoma .
Adenoma, Adrenocortical .
Conn Adenoma .
Conn Disease .
Adenoma, Conn .
Adenomas, Adrenal Cortical .
Adenomas, Adrenocortical .
Adenomas, Conn .
Adrenal Cortical Adenoma .
Adrenal Cortical Adenomas .
Adrenocortical Adenomas .
Conn Adenomas .
Conns Disease .
Disease, Conn .
Disease, Conn's .
Adenoma, Adrenal Cortical .
Conn's Disease .
A benign neoplasm of the ADRENAL CORTEX. It is characterized by a well-defined nodular lesion, usually less than 2.5 cm. Most adrenocortical adenomas are nonfunctional. The functional ones are yellow and contain LIPIDS. Depending on the cell type or cortical zone involved, they may produce ALDOSTERONE; HYDROCORTISONE; DEHYDROEPIANDROSTERONE; and/or ANDROSTENEDIONE. .
0.58
401009
 
Demyelinating Autoimmune Diseases, CNS .
Autoimmune Demyelinating Diseases, CNS .
Autoimmune Demyelinating Diseases, Cerebral .
Autoimmune Demyelinating Diseases, Spinal Cord .
Autoimmune Demyelinating Disorders, CNS .
Autoimmune Diseases, Demyelinating, Brain .
Brain Autoimmune Demyelinating Diseases .
CNS Autoimmune Demyelinating Disorders .
CNS Demyelinating Autoimmune Diseases .
Cerebral Demyelinating Diseases, Autoimmune .
Demyelinating Autoimmune Diseases, Brain .
Demyelinating Autoimmune Diseases, Central Nervous System .
Demyelinating Autoimmune Diseases, Cerebral .
Demyelinating Autoimmune Diseases, Spinal Cord .
Demyelinating Autoimmune Disorders, CNS .
Demyelinating Disease, Autoimmune, CNS .
Autoimmune Demyelinating Diseases, Central Nervous System .
Spinal Cord Demyelinating Autoimmune Diseases .
Conditions characterized by loss or dysfunction of myelin (see MYELIN SHEATH) in the brain, spinal cord, or optic nerves secondary to autoimmune mediated processes. This may take the form of a humoral or cellular immune response directed toward myelin or OLIGODENDROGLIA associated autoantigens. .
0.57
8358
 
Glycogen Storage Disease Type III .
Amylo-1,6-Glucosidase Deficiency .
Cori Disease .
Deficiency, Debrancher .
Glycogen Debrancher Deficiency .
Glycogen Storage Disease III .
Glycogen Storage Disease Type 3 .
Amylo 1,6 Glucosidase Deficiency .
Amylo-1,6-Glucosidase Deficiencies .
Coris Disease .
Debrancher Deficiencies .
Debrancher Deficiencies, Glycogen .
Debrancher Deficiency, Glycogen .
Deficiencies, Amylo-1,6-Glucosidase .
Deficiencies, Debrancher .
Deficiencies, Glycogen Debrancher .
Deficiency, Amylo-1,6-Glucosidase .
Deficiency, Glycogen Debrancher .
Dextrinoses, Limit .
Dextrinosis, Limit .
Disease, Cori .
Disease, Cori's .
Disease, Forbes .
Glycogen Debrancher Deficiencies .
Glycogenosis 3s .
Limit Dextrinoses .
Cori's Disease .
Debrancher Deficiency .
Forbes Disease .
Glycogen Debranching Enzyme Deficiency .
Glycogenosis 3 .
Limit Dextrinosis .
An autosomal recessive metabolic disorder due to deficient expression of amylo-1,6-glucosidase (one part of the glycogen debranching enzyme system). The clinical course of the disease is similar to that of glycogen storage disease type I, but milder. Massive hepatomegaly, which is present in young children, diminishes and occasionally disappears with age. Levels of glycogen with short outer branches are elevated in muscle, liver, and erythrocytes. Six subgroups have been identified, with subgroups Type IIIa and Type IIIb being the most prevalent. .
0.57
1331
 
Brain Diseases .
Brain Disorders .
CNS Disorders, Intracranial .
Central Nervous System Disorders, Intracranial .
Central Nervous System Intracranial Disorders .
Encephalon Diseases .
Encephalopathy .
Intracranial CNS Disorders .
Brain Disease .
Brain Disorder .
CNS Disorder, Intracranial .
Encephalon Disease .
Encephalopathies .
Intracranial CNS Disorder .
Intracranial Central Nervous System Disorders .
Brain Pathology .
Pathologic conditions affecting the BRAIN, which is composed of the intracranial components of the CENTRAL NERVOUS SYSTEM. This includes (but is not limited to) the CEREBRAL CORTEX; intracranial white matter; BASAL GANGLIA; THALAMUS; HYPOTHALAMUS; BRAIN STEM; and CEREBELLUM. .
0.55
63645190