Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Chorea co-occurrent and due to systemic lupus erythematosus |
Is a |
False |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Demyelination of central nervous system co-occurrent and due to systemic lupus erythematosus (disorder) |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Demyelination of central nervous system co-occurrent and due to Sjogren disease (disorder) |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pericarditis secondary to systemic lupus erythematosus |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pediatric onset Sjögren syndrome |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Autosomal systemic lupus erythematosus (disorder) |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Systemic sclerosis |
Is a |
False |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Anti-glomerular basement membrane tubulointerstitial nephritis (disorder) |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Relapsing polychondritis (disorder) |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Drug-induced lupus erythematosus |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal lupus erythematosus |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Lung disease with Sjögren's disease (disorder) |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Rheumatoid episcleritis |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
pneumopathie interstitielle diffuse associée à une polyarthrite rhumatoïde |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Immunoglobulin G4 related kidney disease (disorder) |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Autoimmune interstitial keratitis (disorder) |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare genetic systemic or rheumatologic disease characterized by interstitial lung disease (often with pulmonary hemorrhage) and inflammatory arthritis, associated with high-titer autoantibodies (including anti-nuclear and anti-neutrophil cytoplasmic antibodies, and rheumatoid factor). Patients present from infancy to adolescence with tachypnea, cough, hemoptysis, and/or joint pain. Some patients may also develop glomerular disease. |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Mouth and genital ulcers with inflamed cartilage syndrome (disorder) |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare autoimmune connective tissue disorder characterized by abnormal hardening of the skin and sometimes other organs. It is classified into two main forms: localized scleroderma and systemic sclerosis (SSc), the latter comprising three subsets; diffuse cutaneous SSc (dcSSc), limited cutaneous SSc (lcSSc) and limited SSc (lSSc). Localized scleroderma is the cutaneous form of scleroderma characterized by fibrosis of the skin causing cutaneous plaques (morphea) or strips (linear scleroderma). Systemic sclerosis (SSc) is a generalized disorder characterized by fibrosis and vascular obliteration in the skin and organs, particularly, lungs, heart, and digestive tract. The exact cause of scleroderma is unknown. The disease originates from an autoimmune reaction, which leads to localized overproduction of collagen. In some cases, the condition is associated with exposure to chemicals. Other suggested causes include genetic and infectious mechanisms. |
Is a |
True |
Autoimmune connective tissue disorder |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|