Arthritis

syndrome OMIM 615846

Aicardi-Goutieres Syndrome 7

freq: 1/5 ev: PCS

syndrome OMIM 203500

Alkaptonuria

ev: IEA

syndrome OMIM 616414

Autoimmune Interstitial Lung, Joint, And Kidney Disease

freq: 20/21 ev: PCS

syndrome OMIM 615559

Autoimmune Lymphoproliferative Syndrome, Type Iii

freq: 1/3 ev: PCS

syndrome OMIM 109650

Behcet Syndrome

ev: IEA

syndrome OMIM 208250

Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome

ev: IEA

syndrome OMIM 607115

Chronic Infantile Neurological, Cutaneous, And Articular Syndrome

freq: 9/11 ev: PCS

syndrome OMIM 259100

Cranioosteoarthropathy

ev: IEA

syndrome OMIM 616100

Ctla4 Haploinsufficiency

freq: 2/14 ev: PCS

syndrome OMIM 617772

Deafness, Autosomal Dominant 34, With Or Without Inflammation

ev: IEA

syndrome OMIM 613217

Diarrhea 5, With Tufting Enteropathy, Congenital

freq: HP:0040283 ev: IEA

syndrome OMIM 120100

Familial Cold Autoinflammatory Syndrome 1

freq: 1/1 ev: PCS

syndrome OMIM 611762

Familial Cold Autoinflammatory Syndrome 2

ev: TAS

syndrome OMIM 120100

Familial Cold Urticaria

freq: 1/1 ev: PCS

syndrome OMIM 249100

Familial Mediterranean Fever

freq: 218/561 ev: PCS

syndrome OMIM 228000

Farber Lipogranulomatosis

ev: PCS

syndrome OMIM 602390

Hemochromatosis, Type 2A

ev: TAS

syndrome OMIM 604250

Hemochromatosis, Type 3

ev: TAS

syndrome OMIM 260920

Hyperimmunoglobulinemia D

freq: 40/60 ev: PCS

syndrome OMIM 259100

Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1

ev: IEA

syndrome OMIM 614700

Immunodeficiency, Common Variable, 8, With Autoimmunity

freq: 2/14 ev: PCS

syndrome OMIM 304790

Insulin-Dependent Diabetes Mellitus Secretory Diarrhea Syndrome

freq: 8/88 ev: PCS

phenotype OMIM 304790

Islets of Langerhans, Absence Of

freq: 8/88 ev: PCS

syndrome OMIM 602390

Juvenile Hemochromatosis

ev: TAS

syndrome OMIM 152700

Lupus Erythematosus, Systemic

ev: IEA

syndrome OMIM 210250

Macrothrombocytopenia-Stomatocytosis, Mediterranean

ev: IEA

syndrome OMIM 259100

Osteoarthropathy, Primary Hypertrophic

ev: IEA

syndrome OMIM 615688

Polyarteritis Nodosa, Childhood-Onset

ev: PCS

syndrome OMIM 617591

Proteasome-Associated Autoinflammatory Syndrome 3

ev: IEA

disease OMIM 177900

Psoriasis Susceptibility 1

ev: PCS

syndrome OMIM 604416

Pyogenic Arthritis, Pyoderma Gangrenosum And Acne

freq: 1/1 ev: PCS

syndrome OMIM 613328

Roifman-Chitayat Syndrome

ev: IEA

syndrome OMIM 601457

Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Positive

ev: IEA

disease OMIM 210250

Sitosterolemia

ev: IEA

syndrome OMIM 108300

Stickler Syndrome, Type 1

freq: 15/25 ev: PCS

syndrome OMIM 186580

Synovitis, Granulomatous, With Uveitis And Cranial Neuropathies (Disorder)

freq: 61/66 ev: PCS

disease OMIM 138900

Uric Acid Concentration, Serum, Quantitative Trait Locus 1

ev: IEA

disease OMIM 192950

Vertical Talus

ev: IEA

syndrome OMIM 617321

Yao Syndrome

freq: 41/52 ev: PCS