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familial Mediterranean fever (DOID:2987)
Annotations: Rat: (15) Mouse: (15) Human: (16) Chinchilla: (15) Bonobo: (15) Dog: (16) Squirrel: (14) Pig: (15)
Parent Terms Term With Siblings Child Terms
Aicardi-Goutieres syndrome +   
autoimmune disease of blood +   
autoimmune disease of cardiovascular system +   
autoimmune disease of endocrine system +   
autoimmune disease of exocrine system +   
autoimmune disease of gastrointestinal tract +   
autoimmune disease of musculoskeletal system +   
autoimmune disease of the nervous system +   
autoimmune disease of urogenital tract +   
Autoinflammation with Arthritis and Dyskeratosis  
Autoinflammation with Infantile Enterocolitis  
Autoinflammation, Antibody Deficiency, and Immune Dysregulation, PLCG2-Associated  
autosomal dominant disease +   
autosomal dominant familial periodic fever  
autosomal hemophilia A 
autosomal recessive disease +   
Behcet's disease +   
blepharophimosis, ptosis, and epicanthus inversus syndrome  
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
CINCA syndrome  
congenital nystagmus 1  
Cryopyrin-Associated Periodic Syndromes +   
Deficiency of Interleukin-1 Receptor Antagonist  
exudative vitreoretinopathy 4  
factor XI deficiency  
familial adenomatous polyposis +   
familial Mediterranean fever +   
An autoimmune hypersensitivity disease characterized by recurrent episodes of fever and acute inflammation of the membranes lining the abdomen, joints and lungs; that has_material_basis_in mutations in the MEFV gene, which encodes the protein pyrin. (DO)
Gillespie syndrome  
hypophosphatasia +   
IgG4-related disease  
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome  
Jaccoud's syndrome 
lupus erythematosus +   
McCune Albright syndrome  
mevalonic aciduria  
Periodic Fever, Menstrual Cycle-Dependent  
PFAPA Syndrome  
progeria +   
Proteasome-Associated Autoinflammatory Syndromes +   
Robinow syndrome +   
septooptic dysplasia +   
STING-associated vasculopathy with onset in infancy  
syndromic microphthalmia 12  
syndromic microphthalmia 14  
syndromic microphthalmia 8  
thrombophilia due to thrombomodulin defect  
Vogt-Koyanagi-Harada disease  
Weill-Marchesani syndrome +   

Exact Synonyms: Benign Paroxysmal Peritonitis ;   FAMILIAL PERIODIC FEVER ;   FMF ;   Familial Mediterranean Fever, Autosomal Recessive ;   Familial Paroxysmal Polyserositides ;   Familial Paroxysmal Polyserositis ;   Periodic Disease ;   Periodic Diseases ;   Periodic Fever Syndrome ;   Periodic Peritonitides ;   Periodic Peritonitis ;   Recurrent Polyserositides ;   Recurrent Polyserositis ;   Wolff Periodic Disease ;   Wolff's Periodic Disease ;   Wolffs periodic disease ;   benign paroxysmal peritonitides
Primary IDs: MESH:D010505
Alternate IDs: OMIA:001561 ;   OMIM:249100
Xrefs: GARD:6421 ;   ICD10CM:M04.1 ;   ICD9CM:277.31 ;   NCI:C84707 ;   ORDO:342
Definition Sources: "DO", "DO"

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.