serw-MX  [xml]  

 DeCS Categories

C01 Bacterial Infections and Mycoses .
C01.252 Bacterial Infections .
C01.252.400 Gram-Negative Bacterial Infections .
C01.252.400.780 Rickettsiaceae Infections .
C01.252.400.780.790 Rickettsia Infections .
C01.252.400.780.790.750 Spotted Fever Group Rickettsiosis .
C01.252.400.780.790.750.250 Boutonneuse Fever .
C01.252.400.825 Tick-Borne Diseases .
C01.252.400.825.887 Spotted Fever Group Rickettsiosis .
C01.252.400.825.887.250 Boutonneuse Fever .
C15 Hemic and Lymphatic Diseases .
C15.378 Hematologic Diseases .
C15.378.071 Anemia .
C15.378.071.141 Anemia, Hemolytic .
C15.378.071.141.150 Anemia, Hemolytic, Congenital .
C15.378. Thalassemia .
C15.378. beta-Thalassemia .
C15.378.420 Hemoglobinopathies .
C15.378.420.826 Thalassemia .
C15.378.420.826.150 beta-Thalassemia .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.070 Anemia, Hemolytic, Congenital .
C16.320.070.875 Thalassemia .
C16.320.070.875.150 beta-Thalassemia .
C16.320.365 Hemoglobinopathies .
C16.320.365.826 Thalassemia .
C16.320.365.826.150 beta-Thalassemia .
C16.320.382 Hereditary Autoinflammatory Diseases .
C16.320.382.625 Familial Mediterranean Fever .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.220 Cytoskeletal Proteins .
D12.776.220.909 Pyrin .
D12.776.934 Tripartite Motif Proteins .
D12.776.934.750 Pyrin .
E02 Therapeutics .
E02.642 Nutrition Therapy .
E02.642.249 Diet Therapy .
E02.642.249.270 Diet, Mediterranean .
G07 Physiological Phenomena .
G07.203 Diet, Food, and Nutrition .
G07.203.650 Nutritional Physiological Phenomena .
G07.203.650.240 Diet 3155 .
G07.203.650.240.270 Diet, Mediterranean .
Z01 Geographic Locations .
Z01.756 Oceans and Seas .
Z01.756.592 Mediterranean Sea .
 Synonyms & Historicals
Pyrin .
MEFV Protein .
Marenostrin .
Mediterranean Fever Protein .
TRIM20 Protein .
A tripartite motif protein that consists of an N-terminal pyrin domain, a central coiled-coil region and B-box type ZINC FINGER, and C-terminal regions that mediate homotrimerization and interactions with other proteins (the B30.2/SPRY DOMAIN). It is expressed primarily by mature GRANULOCYTES and associates with the cytoskeleton in the perinuclear area as well as AUTOPHAGOSOMES, where it co-ordinates the assembly of AUTOPHAGY-RELATED PROTEINS and degradation of INFLAMMASOME components. It functions in INNATE IMMUNITY and INFLAMMATION; mutations in the Pyrin protein (MEFV) gene are associated with FAMILIAL MEDITERRANEAN FEVER. .
Familial Mediterranean Fever .
Benign Paroxysmal Peritonitis .
Familial Mediterranean Fever, Autosomal Recessive .
Familial Paroxysmal Polyserositis .
Periodic Peritonitis .
Polyserositis, Familial Paroxysmal .
Polyserositis, Recurrent .
Recurrent Polyserositis .
Benign Paroxysmal Peritonitides .
Disease, Periodic .
Disease, Wolff Periodic .
Disease, Wolff's Periodic .
Diseases, Periodic .
Familial Paroxysmal Polyserositides .
Paroxysmal Peritonitides, Benign .
Paroxysmal Peritonitis, Benign .
Paroxysmal Polyserositides, Familial .
Paroxysmal Polyserositis, Familial .
Periodic Disease, Wolff .
Periodic Disease, Wolffs .
Periodic Diseases .
Periodic Peritonitides .
Peritonitides, Benign Paroxysmal .
Peritonitides, Periodic .
Peritonitis, Benign Paroxysmal .
Peritonitis, Periodic .
Polyserositides, Familial Paroxysmal .
Polyserositides, Recurrent .
Recurrent Polyserositides .
Wolffs Periodic Disease .
Mediterranean Fever, Familial .
Periodic Disease .
Periodic Disease, Wolff's .
Wolff Periodic Disease .
Wolff's Periodic Disease .
A group of HEREDITARY AUTOINFLAMMATION DISEASES, characterized by recurrent fever, abdominal pain, headache, rash, PLEURISY; and ARTHRITIS. ORCHITIS; benign MENINGITIS; and AMYLOIDOSIS may also occur. Homozygous or compound heterozygous mutations in marenostrin gene result in autosomal recessive transmission; simple heterozygous, autosomal dominant form of the disease. .
Boutonneuse Fever .
Rickettsia conorii Infection .
Boutonneuse Fevers .
Fever, Boutonneuse .
Fevers, Boutonneuse .
Infection, Rickettsia conorii .
Infections, Rickettsia conorii .
Rickettsia conorii Infections .
Spotted Fever, Mediterranean .
Mediterranean Spotted Fever .
A febrile disease of the Mediterranean area, the Crimea, Africa, and India, caused by infection with RICKETTSIA CONORII. .
Mediterranean Sea .
An inland sea enclosed by Europe on the west and north, by Asia on the east, and Africa on the south. .
Diet, Mediterranean .
Diets, Mediterranean .
Mediterranean Diets .
Mediterranean Diet .
A diet typical of the Mediterranean region characterized by a pattern high in fruits and vegetables, EDIBLE GRAIN and bread, potatoes, poultry, beans, nuts, olive oil and fish while low in red meat and dairy and moderate in alcohol consumption. .
beta-Thalassemia .
Erythroblastic Anemia .
Mediterranean Anemia .
Microcytemia, beta Type .
Thalassemia Intermedia .
Thalassemia Major (beta-Thalassemia Major) .
Thalassemia Minor (beta-Thalassemia Minor) .
Thalassemia, beta Type .
beta Thalassemia .
Anemia, Cooley .
Anemia, Cooleys .
Anemias, Erythroblastic .
Anemias, Mediterranean .
Cooley's Anemia .
Disease, Hemoglobin F .
Intermedia, Thalassemia .
Intermedias, Thalassemia .
Major, Thalassemia (beta-Thalassemia Major) .
Majors, Thalassemia (beta-Thalassemia Major) .
Mediterranean Anemias .
Microcytemias, beta Type .
Minor, Thalassemia (beta-Thalassemia Minor) .
Minors, Thalassemia (beta-Thalassemia Minor) .
Thalassemia Intermedias .
Thalassemia Major (beta Thalassemia Major) .
Thalassemia Majors (beta-Thalassemia Major) .
Thalassemia Minor (beta Thalassemia Minor) .
Thalassemia Minors (beta-Thalassemia Minor) .
Thalassemia, beta .
Thalassemias, beta .
Thalassemias, beta Type .
Type Microcytemia, beta .
Type Microcytemias, beta .
Type Thalassemia, beta .
Type Thalassemias, beta .
beta Thalassemias .
beta Type Microcytemia .
beta Type Microcytemias .
beta Type Thalassemia .
beta Type Thalassemias .
Anemia, Cooley's .
Anemia, Erythroblastic .
Anemia, Mediterranean .
Hemoglobin F Disease .
Thalassemia Major .
Thalassemia Minor .
A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent. .