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Ontology Browser

Parent Terms Term With Siblings Child Terms
Acquired Pulmonary Alveolar Proteinosis  
Addison's disease +   
Aicardi-Goutieres syndrome +   
Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity  
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis +   
antisynthetase 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 +   
Autoimmune Hypophysitis 
autoimmune interstitial lung, joint, and kidney disease  
autoimmune lymphoproliferative syndrome +   
Autoimmune Progesterone Dermatitis 
Autoinflammation with Arthritis and Dyskeratosis  
Autoinflammation with Episodic Fever and Lymphadenopathy  
Autoinflammation with Infantile Enterocolitis  
Autoinflammation with Pulmonary and Cutaneous Vasculitis  
Autoinflammation, Antibody Deficiency, and Immune Dysregulation, PLCG2-Associated  
Autoinflammation, Immune Dysregulation, and Eosinophilia  
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  
Chediak-Higashi syndrome +   
CINCA syndrome  
Combined Immunodeficiency with Autoimmunity and Spondylometaphyseal Dysplasia  
combined oxidative phosphorylation deficiency 55  
common variable immunodeficiency +   
congenital nystagmus 1  
Cryopyrin-Associated Periodic Syndromes +   
Deficiency of Interleukin-1 Receptor Antagonist  
Diabetes Mellitus, Congenital Autoimmune  
distal arthrogryposis type 1C  
dopamine transporter deficiency syndrome +   
Experimental Autoimmune Uveitis +   
exudative vitreoretinopathy 4  
factor XI deficiency  
familial adenomatous polyposis +   
Familial Autoinflammatory Syndrome, with or without Immunodeficiency  
familial mediterranean fever +   
An autoimmune 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)
focal segmental glomerulosclerosis 3  
Gardner-Diamond Syndrome 
Gillespie syndrome  
hereditary spastic paraplegia 30  
hypophosphatasia +   
IgA glomerulonephritis +   
IgG4-related disease  
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome  
Immunodeficiency 113  
Immunodeficiency 115  
Immunodeficiency 78 with Autoimmunity and Developmental Delay  
Immunodeficiency 85  
Immunodeficiency 87 and Autoimmunity  
Immunodeficiency 89 and Autoimmunity  
Immunodeficiency 94 with Autoinflammation and Dysmorphic Facies  
Immunodeficiency 97 with Autoinflammation  
Immunodeficiency 98 with Autoinflammation, X-Linked  
Jaccoud's syndrome 
Linear IgA Bullous Dermatosis 
McCune Albright syndrome  
membranous glomerulonephritis  
mevalonic aciduria  
Multisystem Autoimmune Disease with Facial Dysmorphism  
Multisystem Autoimmune Disease, Infantile-Onset +   
neurodevelopmental disorder with hypotonia and speech delay  
Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infections 
Periodic Fever, Menstrual Cycle-Dependent  
PFAPA Syndrome  
proteosome-associated autoinflammatory syndrome +   
retinitis pigmentosa 86  
Robinow syndrome +   
septooptic dysplasia +   
Sotos syndrome +   
spondylocostal dysostosis 5  
STING-associated vasculopathy with onset in infancy  
syndromic microphthalmia 12  
syndromic microphthalmia 14  
syndromic microphthalmia 8 
Systemic Autoinflammatory Disease with Vasculitis  
Systemic Autoinflammatory Disease, X-Linked  
thrombophilia due to thrombomodulin defect  
VEXAS syndrome  
Weill-Marchesani syndrome +   
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia  

Exact Synonyms: FAMILIAL PERIODIC FEVER ;   FMF ;   Familial Mediterranean Fever, Autosomal Recessive ;   Familial Paroxysmal Polyserositis ;   Periodic Disease ;   Periodic Fever Syndrome ;   Periodic Peritonitis ;   Wolff periodic disease ;   Wolff's periodic disease ;   Wolffs periodic disease ;   benign paroxysmal peritonitides ;   benign paroxysmal peritonitis ;   familial paroxysmal polyserositides ;   periodic diseases ;   periodic peritonitides ;   recurrent polyserositides ;   recurrent polyserositis
Narrow Synonyms: Familial Mediterranean fever, AR
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", "DO" "DO"

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