Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Adult onset Still's disease |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Sclerodermoid chronic graft-versus-host disease (disorder) |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Diabetic rubeosis |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Progressive nodular histiocytosis |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hemodialysis-associated secondary amyloidosis of skin (disorder) |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Familial chilblain lupus erythematosus |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pigmented purpuric dermatosis (disorder) |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Progressive macular hypomelanosis |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Recurrent venous ulcer of lower limb |
Is a |
False |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Chronic prurigo |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Extragenital lichen sclerosus and morphea (disorder) |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Chronic coalescent cutaneous lobomycosis |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Lipoid dermatoarthritis |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Classical-like Ehlers-Danlos syndrome type 2 |
Is a |
False |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Birt Hogg Dubé syndrome |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Skin changes due to chronic exposure to non-ionizing radiation (disorder) |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Exacerbation of psoriasis (disorder) |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness syndrome (disorder) |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Sun-induced wrinkles |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare hyper-IgE syndrome with characteristics of atopic dermatitis (eczema), chronic mucocutaneous candidiasis, and elevated IgE levels due to ZNF341 deficiency. High plasma levels of IgG and low natural killer (NK) cell numbers are observed. Other major clinical features involve recurrent skin infections with skin abscesses and connective tissue abnormalities. Some patients may have recurrent lung infections. |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome is characterized by the association of multiple sclerosis with lamellar ichthyosis and hematological anomalies (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may include eye involvement (optic atrophy, diplopia), neuromuscular involvement (ataxia, pyramidal syndrome, gait disturbance) and sensory disorder. There have been no further descriptions in the literature since 1992. |
Is a |
True |
Chronic disease of skin |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|