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 DeCS Categories

C01 Bacterial Infections and Mycoses .
C01.252 Bacterial Infections .
C01.252.410 Gram-Positive Bacterial Infections .
C01.252.410.868 Staphylococcal Infections .
C01.252.410.868.820 Staphylococcal Skin Infections .
C01.252.410.868.820.770 Staphylococcal Scalded Skin Syndrome .
C01.252.825 Skin Diseases, Bacterial .
C01.252.825.770 Staphylococcal Skin Infections .
C01.252.825.770.770 Staphylococcal Scalded Skin Syndrome .
C01.539 Infection .
C01.539.100 Arthritis, Infectious .
C01.539.100.500 Arthritis, Reactive .
C01.539.800 Skin Diseases, Infectious .
C01.539.800.720 Skin Diseases, Bacterial .
C01.539.800.720.770 Staphylococcal Skin Infections .
C01.539.800.720.770.770 Staphylococcal Scalded Skin Syndrome .
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 .
C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.900 Spinal Diseases .
C05.116.900.853 Spondylitis .
C05.116.900.853.625 Spondylarthritis .
C05.116.900.853.625.800 Spondylarthropathies .
C05.116.900.853.625.800.637 Arthritis, Reactive .
C05.550 Joint Diseases .
C05.550.114 Arthritis .
C05.550.114.099 Arthritis, Infectious .
C05.550.114.099.500 Arthritis, Reactive .
C05.550.114.122 Arthritis, Juvenile .
C05.550.114.865 Spondylarthritis .
C05.550.114.865.800 Spondylarthropathies .
C05.550.114.865.800.637 Arthritis, Reactive .
C05.799 Rheumatic Diseases .
C05.799.056 Arthritis, Juvenile .
C07 Stomatognathic Diseases .
C07.465 Mouth Diseases .
C07.465.284 Facial Hemiatrophy .
C07.465.299 Facial Nerve Diseases .
C07.465.299.375 Facial Hemiatrophy .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.813 Refsum Disease .
C10.292 Cranial Nerve Diseases .
C10.292.319 Facial Nerve Diseases .
C10.292.319.375 Facial Hemiatrophy .
C10.500 Nervous System Malformations .
C10.500.300 Hereditary Sensory and Motor Neuropathy .
C10.500.300.780 Refsum Disease .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.495 Hereditary Sensory and Motor Neuropathy .
C10.574.500.495.780 Refsum Disease .
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 .
C10.668.829.800.300.780 Refsum Disease .
C12 Male Urogenital Diseases .
C12.777 Urologic Diseases .
C12.777.419 Kidney Diseases .
C12.777.419.815 Renal Tubular Transport, Inborn Errors .
C12.777.419.815.364 Dent Disease .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.351 Female Urogenital Diseases .
C13.351.968 Urologic Diseases .
C13.351.968.419 Kidney Diseases .
C13.351.968.419.815 Renal Tubular Transport, Inborn Errors .
C13.351.968.419.815.364 Dent 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 .
C16.131.666.300.780 Refsum Disease .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.100 Dent Disease .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.375 Hereditary Sensory and Motor Neuropathy .
C16.320.400.375.780 Refsum Disease .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.813 Refsum Disease .
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 .
C16.320.565.663 Peroxisomal Disorders .
C16.320.565.663.760 Refsum Disease .
C16.320.565.861 Renal Tubular Transport, Inborn Errors .
C16.320.565.861.271 Dent Disease .
C17 Skin and Connective Tissue Diseases .
C17.300 Connective Tissue Diseases .
C17.300.775 Rheumatic Diseases .
C17.300.775.049 Arthritis, Juvenile .
C17.800 Skin Diseases .
C17.800.838 Skin Diseases, Infectious .
C17.800.838.765 Skin Diseases, Bacterial .
C17.800.838.765.770 Staphylococcal Skin Infections .
C17.800.838.765.770.770 Staphylococcal Scalded Skin Syndrome .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.813 Refsum Disease .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.813 Refsum Disease .
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 .
C18.452.648.663 Peroxisomal Disorders .
C18.452.648.663.760 Refsum Disease .
C18.452.648.861 Renal Tubular Transport, Inborn Errors .
C18.452.648.861.271 Dent Disease .
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 .
C20.111.198 Arthritis, Juvenile .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Dent Disease .
Dents Disease .
Disease, Dent .
Disease, Dent's .
Disease, Dents .
Dent's Disease .
X-linked recessive NEPHROLITHIASIS characterized by HYPERCALCIURIA; HYPOPHOSPHATEMIA; NEPHROCALCINOSIS; and PROTEINURIA. It is associated with mutations in the voltage-gated chloride channel, CLC-5 (Dent Disease I). Another group of mutations associated with this disease is in phosphatidylinositol 4,5-bisphosphate-5-phosphatase gene. .
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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. .
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391009
 
Arthritis, Reactive .
Arthritis, Post-Infectious .
Post-Infectious Arthritis .
Postinfectious Arthritis .
Reactive Arthritis .
Reiter Disease .
Reiter Syndrome .
Reiter's Disease .
Arthritides, Post-Infectious .
Arthritides, Postinfectious .
Arthritides, Reactive .
Arthritis, Post Infectious .
Disease, Reiter .
Disease, Reiter's .
Post Infectious Arthritis .
Post-Infectious Arthritides .
Postinfectious Arthritides .
Reactive Arthritides .
Reiters Disease .
Syndrome, Reiter .
Arthritis, Postinfectious .
Reiter's Disease .
Reiter Disease .
Reiter Syndrome .
An aseptic, inflammatory arthritis developing secondary to a primary extra-articular infection, most typically of the GASTROINTESTINAL TRACT or UROGENITAL SYSTEM. The initiating trigger pathogens are usually SHIGELLA; SALMONELLA; YERSINIA; CAMPYLOBACTER; or CHLAMYDIA TRACHOMATIS. Reactive arthritis is strongly associated with HLA-B27 ANTIGEN. .
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1203373
 
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. .
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Staphylococcal Scalded Skin Syndrome .
Ritter's Disease .
Staphylococcal Scalded-Skin Syndrome .
Disease, Ritter .
Disease, Ritter's .
Ritters Disease .
Scalded-Skin Syndrome, Staphylococcal .
Scalded-Skin Syndromes, Staphylococcal .
Staphylococcal Scalded-Skin Syndromes .
Syndrome, Staphylococcal Scalded-Skin .
Syndromes, Staphylococcal Scalded-Skin .
Ritter Disease .
Scalded Skin Syndrome, Staphylococcal .
A disease of infants due to group 2 phage type 17 staphylococci that produce an epidermolytic exotoxin. Superficial fine vesicles and bullae form and rupture easily, resulting in loss of large sheets of epidermis. .
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Refsum Disease .
Adult Refsum Disease .
Classic Refsum Disease .
HMSN 4 .
HMSN IV .
Hemeralopia Heredoataxia Polyneuritiformis .
Hereditary Motor And Sensory Neuropathy IV .
Hereditary Motor and Sensory Neuropathy Type IV .
Hereditary Motor and Sensory Neuropathy, Type IV .
Hereditary Type IV Motor and Sensory Neuropathy .
Phytanic Acid Oxidase Deficiency .
Refsum Disease, Adult .
Refsum Disease, Classic .
Refsum Disease, Phytanic Acid Oxidase Deficiency .
Refsum Disease, Phytanoyl-CoA Hydroxylase Deficiency .
Refsum Syndrome .
Refsum's Disease .
Refsum's Syndrome .
Refsum-Thiebaut Syndrome .
Adult Refsum Diseases .
Classic Refsum Diseases .
Disease, Adult Refsum .
Disease, Classic Refsum .
Disease, Refsum .
Disease, Refsum's .
Diseases, Adult Refsum .
Diseases, Classic Refsum .
HMSN IVs .
Heredoataxia Polyneuritiformis, Hemeralopia .
Polyneuritiformis, Hemeralopia Heredoataxia .
Polyneuritiformis, Heredopathia Atactica .
Refsum Disease, Phytanoyl CoA Hydroxylase Deficiency .
Refsum Diseases, Adult .
Refsum Diseases, Classic .
Refsum Thiebaut Syndrome .
Refsum-Thiebaut Syndromes .
Refsums Disease .
Refsums Syndrome .
Syndrome, Refsum .
Syndrome, Refsum's .
Syndrome, Refsum-Thiebaut .
Syndromes, Refsum-Thiebaut .
Heredopathia Atactica Polyneuritiformis .
HMSN Type IV .
Neuropathy, Hereditary Motor and Sensory, Type IV .
Phytanic Acid Storage Disease .
Hereditary-Motor and Sensory-Neuropathy Type IV .
HEREDITARY-MOTOR AND SENSORY NEUROPATHY TYPE IV .
HEREDITARY TYPE IV MOTOR AND SENSORY NEUROPATHY .
NEUROPATHY, HEREDITARY MOTOR AND SENSORY TYPE IV .
REFSUM'S SYNDROME .
REFSUM'S DISEASE .
An autosomal recessive familial disorder that usually presents in childhood with POLYNEUROPATHY; SENSORINEURAL HEARING LOSS; ICHTHYOSIS; ATAXIA; RETINITIS PIGMENTOSA; and CARDIOMYOPATHIES. (From Joynt, Clinical Neurology, 1991, Ch37, p58-9; Rev Med Interne 1996;17(5):391-8) This condition can be caused by mutation in the genes encoding peroxisomal phytanoyl-CoA hydroxylase or proteins associated peroxisomal membrane, leading to impaired catabolism of PHYTANIC ACID in PEROXISOMES. .
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8583
 
Facial Hemiatrophy .
Facial Hemiatrophy of Romberg .
Hemifacial Atrophy, Progressive .
Parry-Romberg Disease .
Parry-Romberg Syndrome .
Progressive Facial Hemiatrophy .
Progressive Hemifacial Atrophy .
Romberg Hemi-Facial Atrophy .
Romberg's Disease .
Atrophies, Hemifacial .
Atrophies, Progressive Hemifacial .
Atrophy, Hemifacial .
Atrophy, Progressive Hemifacial .
Atrophy, Romberg Hemi-Facial .
Disease, Parry-Romberg .
Disease, Romberg .
Disease, Romberg's .
Facial Hemiatrophies .
Facial Hemiatrophies, Progressive .
Facial Hemiatrophy, Progressive .
Hemi-Facial Atrophy, Romberg .
Hemiatrophies, Facial .
Hemiatrophies, Progressive Facial .
Hemiatrophy, Facial .
Hemiatrophy, Progressive Facial .
Hemifacial Atrophies .
Parry Romberg Disease .
Parry Romberg Syndrome .
Progressive Facial Hemiatrophies .
Progressive Hemifacial Atrophies .
Romberg Facial Hemiatrophy .
Romberg Hemi Facial Atrophy .
Rombergs Disease .
Syndrome, Parry-Romberg .
Romberg Disease .
Hemifacial Atrophy .
A syndrome characterized by slowly progressive unilateral atrophy of facial subcutaneous fat, muscle tissue, skin, cartilage, and bone. The condition typically progresses over a period of 2-10 years and then stabilizes. .
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66774
 
Arthritis, Juvenile .
Enthesitis-Related Arthritis, Juvenile .
Juvenile Chronic Arthritis .
Juvenile Idiopathic Arthritis .
Juvenile Rheumatoid Arthritis .
Juvenile-Onset Still Disease .
Juvenile-Onset Stills Disease .
Oligoarthritis, Juvenile .
Polyarthritis, Juvenile, Rheumatoid Factor Negative .
Polyarthritis, Juvenile, Rheumatoid Factor Positive .
Psoriatic Arthritis, Juvenile .
Still Disease, Juvenile-Onset .
Systemic Arthritis, Juvenile .
Arthritis, Juvenile Enthesitis-Related .
Arthritis, Juvenile Psoriatic .
Arthritis, Juvenile Systemic .
Chronic Arthritis, Juvenile .
Enthesitis Related Arthritis, Juvenile .
Idiopathic Arthritis, Juvenile .
Juvenile Arthritis .
Juvenile Enthesitis-Related Arthritis .
Juvenile Oligoarthritis .
Juvenile Onset Still Disease .
Juvenile Onset Stills Disease .
Juvenile Psoriatic Arthritis .
Juvenile Systemic Arthritis .
Juvenile-Onset Still's Disease .
Rheumatoid Arthritis, Juvenile .
Still Disease, Juvenile Onset .
Still's Disease, Juvenile Onset .
Stills Disease, Juvenile-Onset .
Arthritis, Juvenile Chronic .
Arthritis, Juvenile Idiopathic .
Arthritis, Juvenile Rheumatoid .
Still's Disease, Juvenile-Onset .
STILL'S DISEASE .
Arthritis in children, with onset before 16 years of age. The terms juvenile rheumatoid arthritis (JRA) and juvenile idiopathic arthritis (JIA) refer to classification systems for chronic arthritis in children. Only one subtype of juvenile arthritis (polyarticular-onset, rheumatoid factor-positive) clinically resembles adult rheumatoid arthritis and is considered its childhood equivalent. .
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