| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Recurrent herpes simplex |
Is a |
True |
Recurrent infectious disease (disorder) |
Inferred relationship |
Some |
|
| Recurrent upper respiratory tract infection |
Is a |
True |
Recurrent infectious disease (disorder) |
Inferred relationship |
Some |
|
| Recurrent urinary tract infection |
Is a |
True |
Recurrent infectious disease (disorder) |
Inferred relationship |
Some |
|
| Recurrent bacterial infection (disorder) |
Is a |
True |
Recurrent infectious disease (disorder) |
Inferred relationship |
Some |
|
| The reactivation of latent hepatitis C infection usually caused by a medicinal agent, such as an immunosuppressant. |
Is a |
True |
Recurrent infectious disease (disorder) |
Inferred relationship |
Some |
|
| Recurrent skin infection |
Is a |
True |
Recurrent infectious disease (disorder) |
Inferred relationship |
Some |
|
| Recurrent lower respiratory tract infection (disorder) |
Is a |
True |
Recurrent infectious disease (disorder) |
Inferred relationship |
Some |
|
| Recurrent salmonella sepsis co-occurrent with human immunodeficiency virus infection |
Is a |
True |
Recurrent infectious disease (disorder) |
Inferred relationship |
Some |
|
| Recurrent candidiasis of vagina |
Is a |
True |
Recurrent infectious disease (disorder) |
Inferred relationship |
Some |
|
| Recurrent pyogenic cholangitis |
Is a |
True |
Recurrent infectious disease (disorder) |
Inferred relationship |
Some |
|
| Recurrent infection due to specific granule deficiency |
Is a |
True |
Recurrent infectious disease (disorder) |
Inferred relationship |
Some |
|
| Recurrent infection due to immunoglobulin isotype deficiency (disorder) |
Is a |
True |
Recurrent infectious disease (disorder) |
Inferred relationship |
Some |
|
| A rare genetic immune disease characterized by recurrent sinopulmonary infections and autoimmune enterocolopathy, manifesting as frequent episodes of intractable diarrhea with abdominal pain and fever, accompanied by eczematous rashes, due to deficits in components of innate and adaptive immunity. Immunologic abnormalities include IgG subclass deficiency, impaired antigen-induced lymphocyte proliferation, reduced cytokine production by CD8+ T lymphocytes, and decreased numbers of natural killer cells. |
Is a |
True |
Recurrent infectious disease (disorder) |
Inferred relationship |
Some |
|
| A rare genetic immune disease characterized by early onset of recurrent bacterial, viral, and fungal infections, chronic inflammatory bowel disease, gastritis, and inflammatory polyarthritis. Patients present with diarrhea, vomiting, hepatosplenomegaly, mouth ulcers, perianal abscesses, chronic lung disease with bronchiectasis, and failure to thrive. Occurrence of a skin rash associated with lymphocytic vasculitis has also been reported. Immunologic abnormalities include variable T-cell lymphopenia, decreased natural killer cells, and decreased B-cells with variable hypogammaglobulinemia. |
Is a |
True |
Recurrent infectious disease (disorder) |
Inferred relationship |
Some |
|
| A rare hepatic disease characterized by graft infection with the hepatitis B virus (HBV) after liver transplantation, due to persistence and reactivation of HBV in extrahepatic sites (also despite previous clearance of the HBs antigen from serum, as shown by laboratory examination), followed by re-invasion of the graft. It may develop between two weeks and several years post transplantation. Clinico-pathological features are variable and range from mild self-limited hepatitis, chronic active hepatitis, and fulminant hepatitis, to fibrosing cholestatic hepatitis. The condition is associated with significantly reduced graft survival rates and overall patient survival. |
Is a |
True |
Recurrent infectious disease (disorder) |
Inferred relationship |
Some |
|
FHIR