Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Meningococcal rash |
Is a |
False |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Disorder of soft tissue due to diabetes mellitus (disorder) |
Is a |
False |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Familial Mediterranean fever |
Is a |
False |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Glucagonoma syndrome |
Is a |
False |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Acquired epidermolysis bullosa |
Is a |
False |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Pyoderma gangrenosum (disorder) |
Is a |
False |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Acute febrile neutrophilic dermatosis |
Is a |
False |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Nephrogenic systemic fibrosis (disorder) |
Is a |
False |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
CREST syndrome |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Systemic amyloidosis affecting skin (disorder) |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
CRST syndrome |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Immunoglobulin A vasculitis |
Is a |
False |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
A rare autoinflammatory syndrome with characteristics of the presence of features of relapsing polychondritis and Behcet disease in the same individual. This includes cartilage inflammation of the ears, nose, throat and rib cage as well as recurrent oral and genital ulcers respectively. Patients may also present ocular involvement (in particular anterior uveitis or scleritis), arthritis, fever, colitis, thrombophlebitis, and central nervous system vasculitis or in rare cases arterial aneurysms. Symptoms of polychondritis occur secondary to those of Behcet disease in the vast majority of cases. |
Is a |
False |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Cutaneous polyarteritis nodosa |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Severe systemic illness-induced cutaneous atrophy |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Rheumatoid arthritis with nailfold and finger-pulp infarcts (disorder) |
Is a |
False |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Necrotizing vasculitis due to mixed cryoglobulinemia (disorder) |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Lupus erythematosus-associated urticarial vasculitis (disorder) |
Is a |
False |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Drug-induced lymphocytic vasculitis (disorder) |
Is a |
False |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Infantile systemic hyalinosis (ISH) is a very rare disorder belonging to the heterogeneous group of genetic fibromatoses and is characterized by progressive joint contractures, skin abnormalities, severe chronic pain and widespread deposition of hyaline material in many tissues such as the skin, skeletal muscle, cardiac muscle, gastrointestinal tract, lymph nodes, spleen, thyroid, and adrenal glands. |
Is a |
False |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Behcet disease of skin (disorder) |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Mast cell leukemia affecting skin (disorder) |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Cutaneous complication of rheumatoid disease (disorder) |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Systemic onset juvenile chronic arthritis |
Is a |
False |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Adult onset Still's disease |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Crohn's disease of vulva (disorder) |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Crohn's disease of penis (disorder) |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Crohn's disease of scrotum (disorder) |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
A rare genetic disease characterised by infantile or childhood onset of abnormal growth of hyalinised fibrous tissue, giving rise to multiple cutaneous nodules and/or pearly papules predominantly affecting the scalp, ears, neck, face, hands, and feet. Involvement of other organs results in gingival hyperplasia, osteolytic bone lesions, and joint contractures. Some patients exhibit visceral involvement with intractable diarrhoea, increased susceptibility to infections, and severe failure to thrive. |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Crohn's disease of parastomal skin |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
A rare genetic systemic or rheumatologic disease characterized by infantile onset of skin anomalies (such as delayed wound healing with atrophic scars and mild alopecia with dry and brittle hair), retinal rod degeneration with night blindness, degenerative myopathy with muscle weakness, myalgia, and cramps, osteoarthritis, joint laxity, prolapse of internal organs, floating kidney syndrome, malabsorption syndrome, and hypothyroidism. The phenotype has been reported to be more severe in women than in men. |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
A rare genetic autoinflammatory syndrome with skin involvement characterised by cold-induced urticarial rash without angioedema starting in infancy and systemic inflammation due to autosomal dominant mutations in the coagulation factor 12 (F-12) gene. In addition to cold-induced, non-pruritic urticarial rash, patients present with headache, mild to severe arthralgia, fatigue, subfebrile evening temperature, chills, and malaise. Systemic symptoms worsen during the cold season and over the years. |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Bullous systemic lupus erythematosus |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Rash of systemic lupus erythematosus |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Lupus panniculitis |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|
Lupus erythematosus-associated necrotizing vasculitis (disorder) |
Is a |
True |
Systemic disease affecting skin (disorder) |
Inferred relationship |
Some |
|