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Familial Mediterranean Fever
Familial Mediterranean fever
: Causes
Overview
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Related in the Kosmos
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Autoinflammatory syndromes
(9)
Familial cold urticaria
Hyper-IgD and periodic fever syndrome
Muckle wells syndrome
Neonatal onset multisystem inflammatory disease
PAPA syndrome
PAPA syndrome
Tumor necrosis factor receptor associated periodic syndrome
Blau syndrome
Cryopyrin-- associated periodic syndrome
Deficiency of the interleuki- n-1–receptor antagonist
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Rheumatology
Periodic fever syndrome
Hyper-IgD and periodic fever syndrome
Neonatal onset multisystem inflammatory disease
Tumor necrosis factor receptor associated periodic syndrome
Muckle wells syndrome
Mediterranean
Mediterranean sea (oceanography)
Mediterranean forests, woodlands, and shrub
Autosomal recessive disorders
Familial dysautonomia
Friedreich ataxia
Fanconi anemia
Multiple sulfatase deficiency
Mevalonic aciduria
Genetic disorders
(15)
Familial spastic paraparesis
Fibromuscular dysplasia
Familial adenomatous polyposis
Female pseudo-Turner syndrome
Faciocutan- eoskeletal syndrome
Faciocutan- eoskeletal syndrome
Fukuyama type muscular dystrophy
Fetal face syndrome
Fabry disease
Fragile x syndrome
Hyper-IgD and periodic fever syndrome
PAPA syndrome
Friedreich ataxia
Fanconi anemia
Multiple sulfatase deficiency
Mevalonic aciduria
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Diseases and disorders
(55)
Brucellosis
Fasciitis, necrotizing
Floppy mitral valve
Familial dysbetalip- oproteinemia
Fibromyoma
Fibromyoma
Factor x deficiency
Factor v deficiency
Fish tapeworm
Factor vii deficiency
Amyloidosis
Periodic disease
Fast breathing
Symptoms
Rat bite fever
Hereditary periodic fever syndromes
Amyloid
Haemodialy- sis-associated amyloidosis
Primary cutaneous amyloidosis
Familial amyloid neuropathy
Fumarylacetoacetase deficiency disease
PFAPA syndrome
Finnish type amyloidosis
Frambesia tropica
Hyperimmun- oglobulinemia d with periodic fever
Cyclic neutropenia
Senile systemic amyloidosis
Barcoo Fever
Floating harbor syndrome
Hyper-igd syndrome
Myotonic dystrophy type 2
Morvan disease
Factor V Leiden thrombophilia
AL amyloidosis
AA amyloidosis
Lassa fever
Metatropic dwarfism
Funnel chest
Marinesco sjogren syndrome
Meniscus tear
Hemorrhagic fever
Familial spastic paraparesis
Fibromuscular dysplasia
Familial adenomatous polyposis
Female pseudo-Turner syndrome
Faciocutan- eoskeletal syndrome
Fukuyama type muscular dystrophy
Muckle wells syndrome
Familial dysautonomia
Fetal face syndrome
Friedreich ataxia
Fabry disease
Fanconi anemia
Multiple sulfatase deficiency
Fragile x syndrome
Mevalonic aciduria
more...
Skin conditions resulting from errors in metabolism
Familial hypertrigl- yceridemia
Amyloid purpura
Familial dysbetalip- oproteinemia
Amyloidosis
Primary cutaneous amyloidosis
Fabry disease
Coagulation system
(35)
Factor II deficiency
Antithrombin
Bone hemostasis
Clot retraction
Coagulation
Coagulation
Cofact
Des-gamma carboxyprothrombin
Factor IX
Factor VIII
Factor XI
Factor XII
Factor XIII
Factor v deficiency
Factor vii deficiency
Factor x deficiency
Fibrin
Fibrinogenolysis
Hemostasis
High-molec- ular-weight kininogen
Human Activated Protein C
Medical Laboratory Scientist
Platelet
Platelet activation
Prekallikrein
Protein C
Protein S
Protein Z
Protein Z-related protease inhibitor
Prothrombin complex concentrate
Prothrombinase
Tenase
Thrombomodulin
Tissue factor
Tissue factor pathway inhibitor
Von Willebrand factor
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Symptoms
(8)
Fever of unknown origin
Recurrent joint pain
Recurrent abdominal pain recurrent
Abdominal pain
Arthralgia
Arthralgia
Chest pain
Fever
Fast breathing
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Signs and tests
C-reactive protein
Erythrocyte sedimentation rate
Serum haptoglobin
White blood cell count
X-rays
Fibrin
See also
(20)
Fibrosing alveolitis
Fenestrations
Holy League (Mediterranean)
Familial
Relapsing fever
Relapsing fever
Colchicine
Peritonitis
Corsica Channel
Marranos
Feminist Majority Foundation
Fluorhydric acid
Sephardic Jews
Social groups
Adverse impacts of climate change
Gallbladder
MEFV
Myalgia
Host-based intrusion detection system
Paroxysmal
CD2BP1
more...
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